CDC Solutions Expands Global Customer Service with the Appointment of MaryBeth Clark as US Director.Business Editors CHIPPENHAM, UK & PHILADELPHIA--(BUSINESS WIRE)--Sept. 24, 2002 CDC See Control Data, century date change and Back Orifice. CDC - Control Data Corporation Solutions (CDC), (www.cdcsolutions.com), the leading global provider of document-based solutions to the life sciences industries, today announced the appointment of industry professional MaryBeth Clark as Director of US Customer Service. With an extensive background in Regulatory Affairs Regulatory Affairs (RA), also called Government Affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, and banking. Regulatory Affairs professionals usually have responsibility for the following general areas: Based from the company's US office in Conshohocken, PA, Clark will also work directly with CDC Solutions' world headquarters in Chippenham, UK and Vice President of Global Customer Service, Paul Moorhead, to facilitate a united strategy of delivering quality consultancy, support and customer service to CDC's elite group of life sciences customers including such companies as Glaxo SmithKline Consumer Health Care, Boehringer Ingelheim Corporation, Cephalon Ceph´a`lon n. 1. (Zool.) The head. Inc. and Ilex Oncology. Philip Padfield, Chief Executive Officer at CDC Solutions said, "As part of our continued growth, CDC recognized the importance of finding the right individual to direct Customer Service for our expanding US client base. MaryBeth's extensive Regulatory Affairs management background and in-depth understanding of electronic submissions strengthens the core knowledge base and expertise of our outstanding Global Customer Service team. This breadth of experience will enable MaryBeth to successfully manage CDC Solutions' US Customer Service team while, at the same time, draw upon an operational skill set necessary to be a true customer advocate." Since 1992, Clark has been immersed im·merse tr.v. im·mersed, im·mers·ing, im·mers·es 1. To cover completely in a liquid; submerge. 2. To baptize by submerging in water. 3. in electronic documentation and publishing roles within Regulatory Affairs in all tiers of life sciences organizations. In addition to her internal industry experience, Clark served as the Manager of Electronic Submissions at PPD (1) (Parallel Presence Detect) The method used by earlier SIMM memory modules to communicate their capacity to the computer. A binary number coming from a parallel set of pins was read by the system, with each pin representing one bit. Contrast with SPD. , a North Carolina-based Contract Research Organization. Most recently, Clark directed the development and production of electronic and paper submissions, in accordance with global regulatory requirements Regulatory requirements are part of the process of drug discovery and drug development. Regulatory requirements describe what is necessary for a new drug to be approved for marketing in any particular country. including the CTD CTD 1 Connective tissue disease, see there 2 Cumulative trauma disorder, see there and eCTD, at AstraZeneca where she served as the Associate Director of Submissions Management within Regulatory Affairs. Clark was responsible for a total team of 40 production and publishing managers and oversaw o·ver·saw v. Past tense of oversee. the direction of activities that supported all submissions to FDA FDA abbr. Food and Drug Administration FDA, n.pr See Food and Drug Administration. FDA, n.pr the abbreviation for the Food and Drug Administration. . Clark has earned a B.A. in Organizational Dynamics from Immaculata College in Pennsylvania. MaryBeth Clark said, "I am extremely excited to be a part of CDC's Global Customer Service team. The volatility of a regulated life sciences environment makes getting electronic submissions into review a resource intensive and complex task. My goal is to continue to strengthen the US Customer Service team at CDC and to instill in·still v. To pour in drop by drop. in  stil·la tion n. unmatched consistency into customer sites as we deliver world-class solutions." About CDC Solutions Ltd. Founded in 1994, CDC Solutions is the leader in high performance document-based solutions to the life sciences industries. The open, flexible technologies developed by CDC Solutions enable life sciences companies to meet the strict standards of regulatory authorities Noun 1. regulatory authority - a governmental agency that regulates businesses in the public interest regulatory agency administrative body, administrative unit - a unit with administrative responsibilities across the world, helping them achieve quality, accuracy, and data integrity to deliver reports and submissions reliably on time. CDC Solutions helps compress the regulatory submissions and approval process, improving speed to market, cost control, and productivity: all of which contribute to ensuring patients' and physicians' timely access to new drugs. CDC Solutions develops products in-house, employing a team of developers and regulatory specialists who actively pilot new initiatives with clients and partners. Through its strategic business partners, CDC Solutions' technology is used to address the needs of other document intensive industries such as engineering, utilities, and finance. For more information, call +44 1249 705300 (United Kingdom) or +1 610.834.9021 (CDC Solutions Inc., North America North America, third largest continent (1990 est. pop. 365,000,000), c.9,400,000 sq mi (24,346,000 sq km), the northern of the two continents of the Western Hemisphere. ), or visit the CDC Solutions website at www.cdcsolutions.com. CDC Solutions, EZsubs, PDFfusion, PDFrender, PDFaqua, PDFcontrol, Xtensia, Xssembler, and Xport are trademarks or registered trademarks, service marks or registered service marks of CDC Solutions Ltd. All other product and company names mentioned herein may be trademarks of their respective holders. |
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