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STUDY OVERVIEW Concerns about compliance and legal limitations are forcing companies to re-examine how they utilize Medical Science Liasons (MSLs). For many companies under a Corporate Integrity Agreement, there is a greater perceived risk over the next few years when it comes to everything from regulatory bodies to changing industry standards. Best Practices, LLC conducted this study to the provide information on how the roles of MSLs are evolving in the changing pharmaceutical environment and how regulatory concerns are affecting the MSL landscape. This research presents benchmarks around risk factors influencing MSL services in the future, different changes companies are making to MSL policies based on their risk aversion, and the level of support MSLs provide government and advocacy groups. Biopharmaceutical and medical device executives can use this study to determine the best practices for facing the upcoming industry challenges. Note: Data are presented in two segments: The total benchmark class and a U.S. only segment. KEY TOPICS
Industries Profiled: Biotech; Pharmaceutical; Manufacturing; Consumer Products; Diagnostic; Medical Device; Health Care Companies Profiled: Advanced Biohealing; Allergan; Amylin; AstraZeneca; Bayer; Boehringer Ingelheim; Boston Scientific; Cephalon; EndoPharma; Eisai; Gambro; G.E. Healthcare; Genetech; GlaxoSmithKline; Ironwood Pharma; Kadmon Pharma; Laboratorios Esteve; Lantheus Medical Imaging; Metronic; Merck Sharp and Dohme; Novartis; Novo Nordisk; Onyx Pharma; Pfizer; QLT; Quidel; Shire; Takeda; Theravance; UCB
If you purchase Best Practice Database document(s), you will have 30 days from the date of purchase to apply some or all of the cost of the document(s) toward the cost of a Full Access Individual, Pharma, Group or University Membership. Write us at DatabaseTeam@bestpracticesllc.com or call David Guinn at 919-767-9179 if you have any questions.
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