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Best Practice Database
Quality, Compliance and Regulatory » Assuring Quality Programs
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Single User: Authorizes use by the person who places the order or for whom the order was placed.
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Biopharmaceutical and medical device companies spend millions to ensure their products meet quality standards at every stage of the product life cycle. Facing tight budgets and escalating regulations, quality leaders face a balancing act between ensuring product quality and safety and adding value for patients and healthcare providers.
Best Practices, LLC conducted this study to probe ways in which high-performing quality groups are adding value and balancing risk. It addresses how these companies integrate quality into their strategic focus and priorities; use quality dashboards for executive communication; and use learnings from the medical device sector to inform quality improvements at biopharma companies.
Quality leaders can use this study to assess their quality practices, strategic focus, and risk management.
The research employed a data gathering approach that reaps quantitative & qualitative data from
a diverse group of 22 companies. This study includes segmented data for biopharma and medical device companies.
Medical Device; Pharmaceutical; Diagnostic; Manufacturing; Consulting; Biotech; Biopharmaceutical; Health Care; Clinical Research; Laboratories
Boston Scientific; idera pharmaceuticals; Astellas; seracare; GlaxoSmithKline ; GN Hearing; 3M Company; Neopharm; Amgen; NewLink Genetics; Abbvie; Takeda Pharmaceuticals; Daiichi Sankyo; DePuy Synthes; Baxter Healthcare; Novartis; Tesaro; Biogen; Sanofi; Abbott; Medtronic; Beckman Coulter
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.