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West Pharmaceutical Services Inc – ‘10-K’ for 12/31/98

As of:  Thursday, 5/6/99   ·   For:  12/31/98   ·   Accession #:  105770-99-16   ·   File #:  1-08036

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  As Of                Filer                Filing    For·On·As Docs:Size

 5/06/99  West Pharmaceutical Services Inc  10-K       12/31/98   12:372K

Annual Report   —   Form 10-K
Filing Table of Contents

Document/Exhibit                   Description                      Pages   Size 

 1: 10-K        10K98                                                 22±    97K 
 2: EX-3        Amended Articles                                      21     68K 
 3: EX-4        Certificate of Stock                                   3     12K 
 7: EX-10       Asset Purchase Agreement                              68    215K 
 4: EX-10       Bonus Plan                                             2     13K 
 5: EX-10       Designated Exec Officers                               8     32K 
 6: EX-10       Outside Directors                                      6     24K 
 8: EX-13       Annual Report                                         40±   166K 
 9: EX-21       Subsidiaries                                           2     10K 
10: EX-23       Consent Indepen Accts                                  1      7K 
11: EX-24       Power of Attorney                                      9     15K 
12: EX-27       Data Schedule                                          1      7K 


10-K   —   10K98
Document Table of Contents

Page (sequential) | (alphabetic) Top
 
11st Page   -   Filing Submission
4Item l. Business
"Item 2. Properties
"Item 3. Legal Proceedings
"Item 4. Submission of Matters to a Vote of Security Holders
"Item 4 (a). Executive Officers of the Registrant
"Item 5. Market for Registrant's Common Equity and Related Stockholder Matters
"Item 6. Selected Financial Data
"Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations
"Item 7A. Quantitative and Qualitative Disclosure about Market Risk
"Item 8. Financial Statements and Supplementary Data
"Item 9. Changes in and Disagreements With Accountants on Accounting and Financial Disclosure
"Item 10. Directors and Executive Officers of the Registrant
"Item 11. Executive Compensation
"Item 12. Security Ownership of Certain Beneficial Owners and Management
"Item 13. Certain Relationships and Related Transactions
"Item 14. Exhibits, Financial Statement Schedules and Reports on Form 8-K
"Notes to Consolidated Financial Statements
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UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 10-K ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 1998 ---------------- Commission File Number 1-8036 --------- WEST PHARMACEUTICAL SERVICES, INC. -------------------------------------- (Exact name of registrant as specified in its charter) Pennsylvania 23-1210010 ------------------------------------ ------------------- (State or other jurisdiction of (I.R.S. Employer incorporation or organization) Identification Number) 101 Gordon Drive, PO Box 645, Lionville, PA 19341-0645 --------------------------------------------- ---------------- (Address of principal executive offices) (Zip Code) Registrant's telephone number, including area code 610-594-2900 ---------- Securities registered pursuant to Section 12(b) of the Act: Title of each class Name of each exchange on which registered ----------------------------------------------------------------- Common Stock, par value New York Stock Exchange $.25 per share Securities registered pursuant to Section 12(g) of the Act: None ---- Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes X . No . --- --- Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not be contained, to the best of registrant's knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to this Form 10-K.
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As of March 17, 1999, the Registrant had 15,099,072 shares of its Common Stock outstanding. The market value of Common Stock held by non-affiliates of the Registrant as of that date was $514,312,140. Exhibit Index appears on pages F-1, F-2, F-3, and F-4.
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DOCUMENTS INCORPORATED BY REFERENCE ------------------------------------ Documents incorporated by reference: 1) portions of the Registrant's Annual Report to Shareholders for the Company's 1998 fiscal year (the "1998 Annual Report to Shareholders") are incorporated by reference in Parts I and II; and (2) portions of the Registrant's definitive Proxy Statement (the "Proxy Statement") are incorporated by reference in Part III.
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2 PART I Item l. Business -------- The Company ----------- West Pharmaceutical Services, Inc. (formerly The West Company, Incorporated) applies value-added services to the process of bringing new drug therapies and healthcare products to global markets. West's technologies include the design and manufacture of packaging components for pharmaceutical, healthcare and consumer products; the research and development of drug delivery systems, and contract laboratory services and other services that support the manufacturing, filling and packaging of pharmaceutical, healthcare and consumer products. The Company's activities are organized in three operating segments: 1) the Device Product Development segment (consisting of four regional business units serving global markets) designs, manufactures, and sells stoppers, closures, medical device components and assemblies made from elastomers, metal and plastics; 2) the Contract Services segment (consisting of two business units serving the United States and Puerto Rico markets) provides contract manufacturing and contract packaging services to the pharmaceutical and personal care industries and contract laboratory services for testing injectable drug packaging; and 3) the Drug Delivery Research and Development segment (consisting of two business units) identifies and develops drug delivery systems for biopharmaceutical and other drugs to improve their therapeutic performance and/or their method of administration. As of December 31, 1998, the Company and its subsidiaries had 4,800 employees. The Company, a Pennsylvania business corporation, was founded in 1923. The executive offices of the Company are located at 101 Gordon Drive, PO Box 645, Lionville, Pennsylvania 19341-0645, approximately 35 miles from Philadelphia. The telephone number at the Company's executive offices is 610-594-2900. As used in this Item, the term "Company" includes West Pharmaceutical Services, Inc. and its consolidated subsidiaries, unless the context otherwise indicates. Device Product Development Principal Products -------------------------------------------------------- Pharmaceutical Stoppers ----------------------- The Company is the world's largest independent manufacturer of stoppers for sealing drug vials and other pharmaceutical containers. Several hundred proprietary formulations are molded from natural rubber and synthetic elastomers into a variety of 3 stopper sizes, shapes and colors. The stoppers are used in packaging serums, vaccines, antibiotics, anesthetics, intravenous solutions and other drugs. Most stopper formulations are specially designed to be compatible with drugs so that the drugs will remain effective and unchanged during storage. New rubber compounds must be tested to show that they do not leach into the customer's product or affect its potency, sterility, effectiveness, color or clarity. The Company's laboratories conduct tests to determine the compatibility of its stoppers with customers' drugs and, in the United States, file formulation information with the Food and Drug Administration in support of customers' new drug applications. Stoppers usually are washed, sterilized and subject to other pre- use processes by the customer or a third-party before they are fitted on the container. However, the Company has recently introduced a value-added line of stoppers that are pre-washed and ready to be sterilized, eliminating several steps in customers' incoming processes. The Company is also marketing a line of pre- sterilized stoppers that can be introduced directly into customers' sterile drug-filling operations. Metal Seals ----------- The Company also offers a broad line of aluminum seals in various sizes, shapes and colors. The seals are crimped onto glass or plastic pharmaceutical containers to hold the stoppers securely in place. The top of aluminum seals often contains tamper-evident tabs or plastic covers, which must be removed before the drug can be withdrawn. Some aluminum seals are sold with specially formulated rubber or elastomeric discs pre-fitted inside the seal. These "lined" seals may be placed directly onto the pharmaceutical container, thus eliminating the need for a separate stopper. Other Products --------------- Other products for the pharmaceutical industry include: Products used in the packaging of non-injectable drugs such as rubber dropper bulbs, plastic contraceptive drug packages and child-resistant and tamper-evident plastic closures Plastic bottles and containers for the pharmaceutical industry Rubber and plastic components for empty and pre-filled disposable syringes such as plungers, hubs and needle covers 4 Blood-sampling system components, including vacuum tube stoppers and needle valves, and a number of specialized rubber and plastic components for blood-analyzing systems and other medical devices Disposable infant nursers and individual nurser components The Company also manufactures a wide range of standard and custom-designed plastic threaded caps and containers for the personal-care industry. The caps, produced mainly for cosmetics and toiletries, come in many different sizes and colors. The Company also makes closures for food and beverage processors. The Company focuses its efforts on multiple-piece closures that require high-speed assembly. Product Development ------------------------ The Company maintains its own laboratories for testing raw materials and finished goods to assure conformity to customer specifications and to safeguard product quality. Laboratory facilities are also used for development of new products. Engineering staffs are responsible for product and tooling design and testing and for the design and construction of processing equipment. In addition, a corporate product development department develops new packaging and device concepts. Approximately 120 professional employees were engaged full time in these activities in 1998. Development and engineering expenditures for the creation and application of new and improved device products and manufacturing processes were approximately $9.2 million in 1998, $8.8 million in 1997 and $8.9 million in 1996, net of cost reimbursements by customers. Recent Developments ------------------- The Company has taken steps to expand its product offerings and improve competitiveness of its Device Product Development operating segment. The Company increased its capacity in the components area with the acquisition of Schubert Seals A/S, a Danish manufacturer of rubber components and metal seals servicing the European pharmaceutical industry. A 51% ownership interest was acquired in May 1994 and the remaining 49% in December 1995. The company's name was recently changed to "West Pharmaceutical Services Danmark A/S." In 1996 and 1997, the Company implemented a major restructuring plan announced in 1996. The plan included the closing or downsizing of six manufacturing facilities, withdrawal from the machinery business and an approximate 5% reduction in the workforce. The restructuring was designed to reduce the costs associated with multiple plant sites and shift certain production capacity to lower-cost locations. In 1998, a further 1% 5 reduction in the workforce, made possible by manufacturing and other operating efficiencies, was announced. (Additional information pertaining to these activities is incorporated by reference to the Note "Restructuring Charges" of Notes to Consolidated Financial Statements of the 1998 Annual Report to Shareholders.) In 1998, the Company acquired Betraine Limited, a company located in the U.K., which manufactures precision injection molded plastic components for the healthcare and consumer industries. The acquisition expanded global capabilities in the non- injectable market. Contract Services Principal Services -------------------------------- Contract Packaging and Contract Manufacturing --------------------------------------------- The Company entered into the pharmaceutical services market in 1995 with its acquisition of Paco Pharmaceutical Services, Inc. ("Paco"). Paco's name was recently changed to West Pharmaceutical Services Lakewood, Inc. (West Lakewood). West Lakewood provides contract manufacturing and packaging of products for pharmaceutical and consumer-products companies. With its flexible manufacturing environment and workforce, West Lakewood has the capability to quickly undertake to make and package products according to customers' specifications, usually employing customer-supplied raw materials. Once the operation is complete, West Lakewood delivers the finished product to the customer for final sale and distribution to the end user. Customers typically use West Lakewood services on a temporary basis to supplement their own manufacturing or packaging capability during a new-product introduction or special promotion. However, West Lakewood does retain long-term business in both the manufacturing and packaging areas. West Lakewood operates facilities in Lakewood, New Jersey and Canovanas, Puerto Rico. West Lakewood contract packaging and manufacturing processes and services are subject to the Good Manufacturing Practice standards applicable to the pharmaceutical industry as well as to numerous other federal and state laws and regulations governing the manufacture, handling and packaging of drugs and other regulated substances. West Lakewood manufactures liquids and creams, solids, suspensions, and powders. These products produced include: headache and cold medications skin lotions 6 deodorants toothpaste and mouthwash metaproterenol and albuterol, products used for inhalation therapy. West Lakewood contract-packaging services include the design, assembly and filling of a broad variety of packages, including "blister" packages (i.e., a plastic film with a foil backing) bottles and tubes laminated and other flexible pouches or strip packages aluminum and plastic liquid cup containers paperboard specialty packages innovative tamper-evident and child-resistant packages Although the type of package depends on the requirements of the customer, blister packaging or bottles typically are used for tablets and capsules while aluminum or plastic cups, pouches, bottles and tubes are used for liquids, creams, ointments and powders. Contract Laboratory Services ----------------------------- In 1998, the Company established the contract laboratory services business, which provides testing services to analyze customers' injectable product packaging. Regulatory agencies require drug companies to demonstrate that packaging components will not contaminate the drug. The test data is generated in a format acceptable for U.S. Food and Drug Administration (FDA) submissions. The services offered include product/closure interaction testing, extractables testing, moisture analysis of closures, particle quantification/analysis, quantification of closure surface silicone, and other custom services. The Company's laboratory complies with applicable Good Manufacturing Practice standards and its laboratory will be FDA registered. Research and Development Drug Delivery Systems --------------------------------------------------------- In 1993, the Company began developing drug-delivery systems for bio-pharmaceuticals and other drugs that are difficult to administer effectively through traditional injectable or oral routes. Improving the therapeutic performance of these drugs in an economical fashion calls for sophisticated delivery solutions. 7 To advance the Company's efforts in this area, in 1994 the Company began acquiring interests in DanBioSyst UK Ltd. (DBS) in 10% annual increments; and in March 1998, acquired the remaining 70% ownership interest, making DBS a wholly-owned subsidiary. DBS is a research company located in Nottingham, England, which specializes in identifying and developing systems for delivery of complex drug molecules, or to assist in delivering drugs to a specific site in the body. DBS engages in research to develop these unique systems and then patents this technology. DBS has patents or patent applications covering a range of delivery platforms including nasal, oral, parenteral, pulmonary and rectal/vaginal. DBS enters into agreements with biopharmaceutical and other drug companies, to apply its delivery system technology to the customers' drug molecule to achieve the desired result. The Company's Lionville-based resources are dedicated to development of drug delivery systems. This group's work, until recently, was focused on the Ocufit SR system, a silicone rod small enough to fit behind the eyelid. The Ocufit SR can be designed to release a number of different drugs in predefined quantities over time periods ranging from two weeks to several months without physical intervention. The Ocufit SR is being jointly developed with Escalon Medical Corporation, which owns the basic technology. An Investigative New Drug Application was filed with the FDA late in 1998, and Escalon is now conducting Phase I clinical trials. The Lionville group is also developing products based on DBS patented technology. The current projects relate to nasal delivery of leuprolide and morphine and further development of the Targit delivery system, a coated starch capsule, designed to deliver medication to a specific site in the body. The Company had 58 employees directly engaged in these activities as of December 31, 1998 and total expenses were $5.3 million, net of revenues received, in 1998. Order Backlog -------------- Device product orders on hand at December 31, 1998 were approximately $90 million, compared with approximately $80 million at the end of 1997. Orders on hand include those placed by customers for manufacture over a period of time according to a customer's schedule or upon confirmation by the customer. Orders are generally considered firm when goods are manufactured or orders are confirmed. The Company also has contractual arrangements with a number of its customers, and products covered by these contracts are included in the Company's backlog only as orders are received from those customers. West Lakewood's twelve-month backlog of unfilled customer orders was approximately $18 million at December 31, 1998 and December 31, 1997. Backlog is defined by West Lakewood as orders written 8 and included in production schedules during the next 12 months. Such orders generally may be cancelled by the customer without penalty. Raw Materials -------------- The Company uses three basic raw materials in the manufacture of its device products: rubber; aluminum; and plastic. The Company has been receiving adequate supplies of raw materials to meet its production needs, and it foresees no significant availability problems in the near future. The Company is pursuing a supply chain management strategy, which involves purchasing from integrated suppliers that control their own sources of supply. This strategy has reduced the number of raw-materials suppliers used by the Company. In some cases, the Company will purchase raw materials from a single source to assure quality and reduce costs. This strategy increases the risks that the Company's supply lines may be interrupted in the event of a supplier production problem. These risks are managed by selecting suppliers with multiple manufacturing sites, rigid- quality control systems, surplus inventory levels and other methods of maintaining supply in case of interruption in production. Patents and Licenses --------------------- The Company's device products patents and trademarks have been useful in establishing the Company's market share and in the growth of the Company's manufactured device product business and may continue to be of value in the future, especially in view of the Company's continuing development of its own proprietary products. Nevertheless, the Company does not consider its current manufactured device product business or its earnings to be materially dependent upon any single patent or trademark. Although not material at this time, the Company believes its drug delivery development capabilities will play an increasingly important role in the future. DBS has a growing portfolio of patented technology, which is critical to our success because a significant amount of future income is expected to be derived from licensing this technology to customers. Major Customers ----------------- The Company provides manufactured device components and/or contract services to major pharmaceutical and hospital supply/medical device companies, many of which have several divisions with separate purchasing responsibilities. The Company also provides contract-packaging and contract-manufacturing services for many of the leading manufacturers of personal-care products. The Company distributes its products and services 9 primarily through its own sales force but also uses regional distributors in the United States and Asia/Pacific. The business units have separate sales forces but the Company is increasing the sales effort of each group to sell all of the Company's capabilities. Becton Dickinson and Company ("B-D") accounted for approximately 12% of the Company's 1998 consolidated net sales. The principal products sold to B-D are synthetic rubber, natural rubber, metal and plastic components used in B-D's disposable syringes and blood sampling and analysis devices. The Company expects to continue as a major B-D supplier. Excluding B-D, the next ten largest customers accounted for approximately 30% of the Company's consolidated net sales in 1998, but no one of these customers accounted for more than 5% of 1998 consolidated net sales. Competition ------------ The Company competes with several companies, some of which are larger than the Company, across its major Device Product Development product lines. In addition, many companies worldwide compete with the Company for business related to specific product lines. However, the Company believes that it supplies a major portion of the U.S. market requirements for pharmaceutical elastomer and metal packaging components and has a significant share of the European market for these components. Because of the special nature of these products, competition is based primarily on product design and performance, although total cost is becoming increasingly more important as pharmaceutical companies initiate aggressive cost-control measures across their entire operations. Competitors often compete on the basis of price. The Company differentiates itself from its competition as a "full-service" supplier, which is able to provide pre-sale compatibility studies and other services and sophisticated post- sale technical support on a global basis. The Company competes against numerous competitors in the field of plastic closures for consumer products, many of which are larger than the Company and command dominant market shares. The Company attempts to differentiate itself through its expertise in high- speed assembly of multiple-piece closures. The U.S. contract-packaging and manufacturing service industry is highly competitive. For packaging services, West Lakewood competes with three significant companies, only two of which are larger than it. For contract-manufacturing services, West Lakewood competes with four major competitors and several smaller regional companies; several of these competitors are larger than it. In addition, most domestic pharmaceutical companies maintain in-house manufacturing and packaging capabilities and at times will offer their excess capacity to manufacture or package other 10 companies' products on a contract basis. However, most large pharmaceutical and personal healthcare companies have traditionally made extensive use of contract packagers and manufacturers during times of peak demand, during the introduction of a new product and for production of samples and special product promotions. Many companies provide proprietary drug delivery technologies to the pharmaceutical and biotech markets. However, unlike West, the majority of these companies are focused on a single route of drug administration, and very few have capabilities necessary to take drug products through all stages of the development process and commercial manufacture. The three largest companies, the market leaders, have multiple-delivery technologies, but their strong franchises are in oral, controlled-release delivery systems. West's drug delivery technologies, none of which is currently in commercial production, are in less competitive segments that do not compete with the market leaders. Environmental Regulations --------------------------------------------------- The Company does not believe that it will have any material expenditures relating to environmental matters other than those discussed in the Note "Commitments and Contingencies" of Notes to Consolidated Financial Statements of the 1998 Annual Report to Shareholders, incorporated by reference herein. International --------------- The Note "Affiliated Companies" and the Note "Segment Information" of Notes to Consolidated Financial Statements of the 1998 Annual Report to Shareholders are incorporated herein by reference. The Company believes that its international business does not involve a substantially greater business risk than its domestic business. Financial crises in the Asia/Pacific region and more recently in our major markets in South America have resulted in a decline in demand for the Company's products in these regions; however, direct sales to customers in these markets have historically not been significant, representing less than 10% of consolidated sales. The Company's financial condition and results are impacted by fluctuations in exchange-rate markets (See Notes "Summary of Significant Accounting Policies - Foreign Currency Translation" and "Other Income (Expense)" of Notes to Consolidated Financial Statements of the 1998 Annual Report to Shareholders, incorporated herein by reference). Hedging by the Company of these exposures is discussed in the Note "Debt" and in the Note "Financial Instruments" of Notes to Consolidated Financial 11 Statements of the 1998 Annual Report to Shareholders, incorporated herein by reference. Item 2. Properties ----------- In the Device Product Development operating segment, the Company maintains nine manufacturing plants and two mold and die production facilities in the United States, one manufacturing plant in Puerto Rico, and a total of eight manufacturing plants and two mold and die production facilities in Germany, England, France, Denmark, Brazil and Singapore. In the Contract Services operating segment, the Company maintains one facility in the United States and one facility in Puerto Rico to provide contract manufacturing and packaging services. Contract Laboratory services are provided from the Company's Lionville, Pennsylvania facility. The Company's executive offices, U.S. research and development center and pilot plant are located in a leased facility at Lionville, Pennsylvania, about 35 miles from Philadelphia. The Company conducts drug delivery research and development in a leased facility located in Nottingham, England. All other company facilities are used for manufacturing and distribution, and facilities in Eschweiler, Germany are also used for device product development activities. The production facilities of the Company are well-maintained, are operating generally on a two- or three-shift basis and are adequate for the Company's present needs. The principal facilities in the United States and Puerto Rico are as follows: - Approximately 839,000 square feet of owned and 997,000 square feet of leased space in Pennsylvania, New Jersey, Florida, Nebraska, North Carolina and Puerto Rico. The principal international facilities are as follows: - Approximately 530,000 square feet of owned space and 67,700 square feet of leased space in Germany, England, Denmark and France. - Approximately 69,000 square feet of owned space in Brazil. - Approximately 92,000 square feet of owned space in Singapore. Of the aforementioned currently owned facilities, approximately 354,000 square feet are subject to mortgages to secure the Company's real estate mortgage notes. See the Note "Debt" of Notes to Consolidated Financial Statements of the 1998 Annual 12 Report to Shareholders, which information is incorporated herein by reference. Sales office facilities in separate locations are leased under short-term arrangements. The Company also holds for sale former manufacturing facility space in Puerto Rico - totaling 42,000 square feet. Item 3. Legal Proceedings. ----------------- None 13 Item 4. Submission of Matters to a Vote of Security Holders --------------------------------------------------- None. Item 4 (a) Executive Officers of the Registrant ----------------------------------------- The executive officers of the Company at March 31, 1999 were as follows: [Download Table] Name Age Business Experience During Past Five Years ---- --- --------------------------------------- George R. Bennyhoff1 55 Senior Vice President, Human Resources and Public Affairs. Jerry E. Dorsey1 54 President and Chief Operating Officer since September 1998, previously Executive Vice President and Chief Operating Officer from June 1994 to August 1998; Group President from August 1993 to June 1994; President, Health Care Division from May 1992 to July 1993 for the Company. Steven A. Ellers1 48 Senior Vice President and Chief Financial Officer since March 1998; previously Group President from August 1997 to February 1998; Corporate Vice President, Sales from April 1996 to July 1997; Vice President, Operations from June 1994 to March 1996; Vice President Asia/Pacific and Managing Director, Singapore from May 1990 to May 1994 for the Company. John R. Gailey III1 44 Vice President since December 1995, General Counsel since May 1994 and Secretary. Stephen M. Heumann1 57 Vice President since May 1994 and Treasurer. Lawrence P. Higgins1 59 Vice President, Operations since May 1996 and prior to joining the Company an international business consultant from 1994 to 1996 and Senior Vice President International Operations for Revlon, Inc., a cosmetics company, from 1992 to 1994. 1 Holds position as corporate officer elected by the Board of Directors for one year term. 14 Name Age Business Experience During Past Five Years ---- --- --------------------------------------- William G. Little1 56 Chairman of the Board since May 1995, Director and Chief Executive Officer for the Company and President of the Company until September 1998. Donald E. Morel, Jr.1 41 Group President since March 1998; previously, Corporate Vice President, Scientific Services from May 1995 to February 1998; Vice President, Research & Development from August 1993 to May 1995 and prior thereto Director Research & Development, Health Care Products Division from May 1993 to August 1993 for the Company. Anna Mae Papso1 55 Vice President and Corporate Controller Anthony A. Sinkula 61 Vice President and Chief Scientific Officer since July 1998 and prior to joining the Company a consultant to several major pharmaceutical companies and the National Cancer Institute. 1 Holds position as corporate officer elected by the Board of Directors for one year term. 15 PART II Item 5. Market for Registrant's Common Equity and Related Stockholder Matters -------------------------------------------------- The Company's common stock is listed on the New York Stock Exchange and the high and low prices for the stock for each calendar quarter in 1998 and 1997 were as follows: [Download Table] First Second Third Fourth Quarter Quarter Quarter Quarter Year High Low High Low High Low High Low High Low 1998 321/4 2815/16 33 28 30 25 3511/16 27 3511/16 25 1997 291/4 27 30 27 343/16 281/2 351/16 28 351/16 27 As of December 31, 1998, the Company had 1,903 shareholders of record. There were also 2,900 holders of shares registered in nominee names. The Company's common stock paid a quarterly dividend of $.14 per share in each of the first three quarters of 1997; $.15 per share in the fourth quarter of 1997 and each of the first three quarters of 1998; and $.16 per share in the fourth quarter of 1998. Item 6. Selected Financial Data. ----------------------- Information with respect to the Company's net sales, income (loss) from consolidated operations, income (loss) before change in accounting method, income (loss) before change in accounting method per share (basic and assuming dilution) and dividends paid per share is incorporated by reference to the line items corresponding to those categories under the heading "Ten-Year Summary - Summary of Operations" of the 1998 Annual Report to Shareholders. Information with respect to total assets and total debt is incorporated by reference to the line items corresponding to those categories under the heading "Ten-Year Summary - Year- End Financial Position" of the 1998 Annual Report to Shareholders. Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations. --------------------------------------------------------- The information called for by this Item is incorporated by reference to the text appearing in the "Financial Review" section of the 1998 Annual Report to Shareholders. Item 7A. Quantitative and Qualitative Disclosure about Market Risk -------------------------------------------------------- The information called for by this Item is incorporated by reference to the Notes "Financial Instruments", "Summary of Significant Accounting Policies" of Notes to Consolidated Financial Statements of the 1998 Annual Report to Shareholders. 16 Item 8. Financial Statements and Supplementary Data. ------------------------------------------- The information called for by this Item is incorporated by reference to "Consolidated Financial Statements", "Notes to Consolidated Financial Statements", and "Quarterly Operating and Per Share Data (Unaudited)" of the 1998 Annual Report to Shareholders. Item 9. Changes in and Disagreements With Accountants on Accounting and Financial Disclosure. ------------------------------------------------------- None. PART III Item 10. Directors and Executive Officers of the Registrant. --------------------------------------------------- Information called for by this Item is incorporated by reference to "PROPOSAL #1: ELECTION OF DIRECTORS" and "OWNERSHIP OF COMPANY STOCK" in the Proxy Statement. Information about executive officers of the Company is set forth in Item 4 (a) of this report. Item 11. Executive Compensation. ----------------------- Information called for by this Item is incorporated by reference to "INFORMATION ABOUT THE BOARD AND BOARD COMMITTEES - Compensation of Directors"; "BOARD COMPENSATION COMMITTEE REPORT ON EXECUTIVE COMPENSATION"; and "COMPENSATION OF NAMED EXECUTIVE OFFICERS" contained in the Proxy Statement. Item 12. Security Ownership of Certain Beneficial Owners and Management. --------------------------------------------------- Information called for by this Item is incorporated by reference to "OWNERSHIP OF COMPANY STOCK" contained in the Proxy Statement. Item 13. Certain Relationships and Related Transactions. ----------------------------------------------- None PART IV Item 14. Exhibits, Financial Statement Schedules and Reports on Form 8-K. ------------------------------------------------------- (a) 1. The following report and consolidated financial statements, included in the 1998 Annual Report to Shareholders, have been incorporated herein by reference: 17 Consolidated Statements of Income for the years ended December 31, 1998, 1997 and 1996 Consolidated Statements of Comprehensive Income for the years ended December 31, 1998, 1997 and 1996 Consolidated Balance Sheets at December 31, 1998 and 1997 Consolidated Statements of Shareholders' Equity for the years ended December 31, 1998, 1997 and 1996 Consolidated Statements of Cash Flows for the years ended December 31, 1998, 1997 and 1996 Notes to Consolidated Financial Statements Report of Independent Accountants (a) 2. Supplementary Financial Information Schedules are omitted because they are either not applicable, not required or because the information required is contained in the consolidated financial statements or notes thereto. (a) 3. See Index to Exhibits on pages F-1, F-2, F-3 and F-4 of this Report. (b) There were no reports on Form 8-K filed by the Company in the fourth quarter of 1998. (c) The exhibits are listed in the Index to Exhibits on pages F-1, F-2, F-3 and F-4 of this Report. (d) Financial Statements of affiliates are omitted because they do not meet the tests of a significant subsidiary at the 20% level. 18 SIGNATURES Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, West Pharmaceutical Services, Inc. has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized. WEST PHARMACEUTICAL SERVICES, INC. (Registrant) By /s/ Steven A. Ellers -------------------------------- Steven A. Ellers Senior Vice President and Chief Financial Officer March 31, 1999 -------------------------------- Date Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons in the capacities and on the dates indicated. [Download Table] Signature Title Date --------- ------ ------- William G. Little Chairman, Director March 31, 1999 --------------------------------- and Chief Executive William G. Little Officer (Principal Executive Officer) Tenley E. Albright Director March 31, 1999 ----------------------------------- Tenley E. Albright * John W. Conway Director March 31, 1999 ___________________________________ John W. Conway* George W. Ebright Director March 31, 1999 ------------------------------------ George W. Ebright* Steven A. Ellers Senior Vice President March 31, 1999 ------------------------------------ and Chief Financial Steven A. Ellers Officer L. Robert Johnson Director March 31, 1999 ------------------------------------ L. Robert Johnson* William H. Longfield Director March 31, 1999 -------------------------------------- William H. Longfield* 20 Signature Title Date --------- ------ ------- John P. Neafsey Director March 31, 1999 -------------------------------------- John P. Neafsey* Anna Mae Papso Vice President March 31, 1999 -------------------------------------- and Corporate Controller Anna Mae Papso (Principal Accounting Officer) Director March 31, 1999 --------------------------------------- Monroe E. Trout Anthony Welters Director March 31, 1999 --------------------------------------- Anthony Welters* J. Roffe Wike, II Director March 31, 1999 --------------------------------------- J. Roffe Wike, II* Geoffrey F. Worden Director March 31, 1999 ---------------------------------------- Geoffrey F. Worden* * By William G. Little pursuant to a power of attorney. 21 INDEX TO EXHIBITS [Download Table] Exhibit Number (3) (a) Amended and Restated Articles of Incorporation of the Company through January 4, 1999. (3) (b) Bylaws of the Company, as amended through October 27, 1998, incorporated by reference to Exhibit (3)(b) to the Company's Form 10-Q for the quarter ended September 30, 1998 (File No. 1-8036). (4) (a) Form of stock certificate for common stock. (4) (b) Flip-In Rights Agreement between the Company and American Stock Transfer & Trust Company, as Rights Agent, dated as of January 16, 1990, incorporated by reference to Exhibit 1 to the Company's Form 8-A Registration Statement (File No. 1-8036). (4) (c) Flip-Over Rights Agreement between the Company and American Stock Transfer & Trust Company, as Rights Agent, dated as of January 16, 1990, incorporated by reference to Exhibit 2 to the Company's Form 8-A Registration Statement (File No. 1-8036). (9) None. (10) (a) Lease dated as of December 31, 1992 between Lion Associates, L.P. and the Company, relating to the lease of the Company's headquarters in Lionville, Pa., incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1992 (File No. 1-8036). (10) (b) First Addendum to Lease dated as of May 22, 1995 between Lion Associates, L.P. and the Company, incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1995 (File No. 1-8036). (10) (c) Long-Term Incentive Plan, as amended March 2, 1993, incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1992 (File No. 1- 8036). (10) (d) Amendments to the Long Term Incentive Plan, dated April 30, 1996, incorporated herein by reference to the Company's Form 10Q for the quarter ended June 30, 1996 (File No. 1- 8036). (10) (e) Executive Incentive Bonus Plan 1999. 22 F - 1 Exhibit Number (10) (f) Non-Qualified Stock Option Plan for Non-Employee Directors, reflecting amendments effective April 30, 1996 and April 28, 1998 incorporated by reference to the Company's Quarterly Report on Form 10-Q for the quarter ended March 31, 1998 (File No. 1-8036). (10) (g) Form of amended and restated agreement between the Company and certain of its executive officers, incorporated by reference to the Company's Quarterly Report on Form 10-Q for the quarter ended March 31, 1998 (File No.1-8036). (10) (h) Schedule of agreements with executive officers, incorporated herein by reference to the Company's Quarterly Report on Form 10Q for the quarter ended March 31, 1998 (File No.1-8036). (10) (i) Supplemental Employees' Retirement Plan, incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1989 (File No. 1-8036). (10) (j) Amendment No. 1 to Supplemental Employees' Retirement Plan, incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1995 (File No. 1- 8036). (10) (k) Amendment No. 2 to Supplemental Employees' Retirement Plan, incorporated by reference to the Company's Quarterly Report on Form 10-Q for the period ended September 30, 1995 (File No. 1-8036). (10) (l) Retirement Plan for Non-Employee Directors of the Company, as amended April 28, 1998, incorporated by reference to the Company's Quarterly Report on Form 10-Q for the quarter ended March 31, 1998 (File No. 1-8036). (10) (m) Employment Agreement dated May 20, 1991 between the Company and William G. Little, incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1991 (File No. 1-8036). (10) (n) Non-Qualified Deferred Compensation Plan for Designated Executive Officers and Amendments Nos. 1 and 2 thereto. (10) (o) Non-qualified Deferred Compensation Plan for Outside Directors and Amendment No. 1 thereto. 23 F - 2 Exhibit Number (10) (p) Lease Agreement, dated August 31, 1978, between Paco Packaging, Inc. and Nineteenth Lakewood Corp., as amended by Amendment of Lease, dated November 30, 1978, Second Amendment of Lease, dated August 6, 1979, Third Amendment of Lease, dated July 24, 1980 and Fourth Amendment of Lease, dated August 14, 1980, incorporated by reference to the Exhibits to Paco Pharmaceutical Services, Inc's Registration Statement on Form S-1, Registration No. 33- 48754, filed with the Commission. (10) (q) Fifth Amendment of Lease, dated May 13, 1994, to the Lease Agreement, dated August 31, 1978, between Paco Packaging, Inc. and Nineteenth Lakewood Corp., incorporated by reference to the Exhibits to Paco Pharmaceutical Services, Inc.'s Annual Report on Form 10-K for the year ended March 31, 1994 (File number 0-20324). (10) (r) Lease Agreement, dated December 9, 1977, between Paco Packaging, Inc. and New Oak Street Corp., as amended by the Amendment to Lease Agreement, dated August 31, 1978, Second Amendment of Lease, dated April 8, 1979 and Third Amendment of Lease, dated November 16, 1983, incorporated by reference to the Exhibits to Paco Pharmaceutical Services, Inc.'s Registration Statement on Form S-1, Registration No. 33-48754, filed with the Commission. (10) (s) Lease Agreement, dated April 7, 1986, between Northlake Realty Co. Inc. and Paco Packaging, Inc., as amended by Amendment to Lease, dated July 1, 1986, Second Amendment of Lease, dated June 15, 1987 between Paco Packaging and C. P. Lakewood, L. P., Agreement, dated December 29, 1987, and Lease Modification Agreement, dated December 13, 1989, incorporated by reference to the Exhibits to Paco Pharmaceutical Services, Inc.'s Registration Statement on Form S-1, Registration No. 33-48754, filed with the Commission. (10) (t) Collective Bargaining Agreement, dated December 1, 1997, by and between Paco Pharmaceutical Services, Inc. and Teamster Local 35 (affiliated with the International Brotherhood of Teamsters), incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1997 (File No.1-8036). (10) (u) 1998 Key Employee Incentive Compensation Plan, dated March 10, 1998, incorporated by reference to the Company's Annual Report on Form 10-K for the year ended December 31, 1997 (File No.1-8036). (10) (v) Asset Purchase Agreement Among Collaborative Clinical Research, Inc., GFI Pharmaceutical Services, Inc., and WCE clinical Evaluations and West Pharmaceuticals, Inc. dated December 28, 1998. 24 F - 3 Exhibit Number (11) Not Applicable. (12) Not Applicable. (13) Portions of 1998 Annual Report to Shareholders. (16) Not applicable. (18) None. (21) Subsidiaries of the Company. (22) None. (23) Consent of Independent Accountants. (24) Powers of Attorney. (27) Financial Data Schedules (99) None. F - 4

Dates Referenced Herein   and   Documents Incorporated by Reference

Referenced-On Page
This ‘10-K’ Filing    Date First  Last      Other Filings
5/7/99
Filed on:5/6/99
3/31/99410-Q
3/17/992
1/4/994
For Period End:12/31/9814
12/28/984
10/27/984
9/30/98410-Q
4/28/984
3/31/98410-Q,  NT 10-K
3/10/984
12/31/97410-K,  NT 10-K
12/1/974
12/31/96410-K
6/30/96410-Q
4/30/964DEF 14A
12/31/95410-K
9/30/95410-Q
5/22/954
5/13/94410-Q
3/31/94410-Q
3/2/934
12/31/924
 List all Filings 


15 Subsequent Filings that Reference this Filing

  As Of               Filer                 Filing    For·On·As Docs:Size             Issuer                      Filing Agent

 4/25/24  West Pharmaceutical Services Inc. 10-Q        3/31/24   85:26M
 2/20/24  West Pharmaceutical Services Inc. 10-K       12/31/23  127:35M
10/26/23  West Pharmaceutical Services Inc. 10-Q        9/30/23   86:9.4M
 7/27/23  West Pharmaceutical Services Inc. 10-Q        6/30/23   86:8.9M
 4/27/23  West Pharmaceutical Services Inc. 10-Q        3/31/23   85:7.6M
 2/21/23  West Pharmaceutical Services Inc. 10-K       12/31/22  122:16M
10/27/22  West Pharmaceutical Services Inc. 10-Q        9/30/22   82:9.8M
 7/28/22  West Pharmaceutical Services Inc. 10-Q        6/30/22   83:9.6M
 4/28/22  West Pharmaceutical Services Inc. 10-Q        3/31/22   84:7.8M
 2/22/22  West Pharmaceutical Services Inc. 10-K       12/31/21  124:27M                                    Workiva Inc Wde… FA01/FA
10/28/21  West Pharmaceutical Services Inc. 10-Q        9/30/21   83:9.7M
 7/30/21  West Pharmaceutical Services Inc. 10-Q        6/30/21   82:9.3M
 4/30/21  West Pharmaceutical Services Inc. 10-Q        3/31/21   83:7.7M
 2/23/21  West Pharmaceutical Services Inc. 10-K       12/31/20  129:17M
10/23/20  West Pharmaceutical Services Inc. 10-Q        9/30/20   87:11M
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