A new report from Medical Device Daily examines regulatory, litigation and enforcement issues in the med-tech development process, along with their implications, case studies and an assessment of best practices and what-not-to-do guidance.

Laws govern the development medical devices and drugs, and no amount of business instinct can substitute for knowledge of the law. Maneuvering through such profoundly regulated markets requires facts, not luck, and this report delivers that indispensable information.

At 500 pages, Drug & Device Litigation & Enforcement: Key Cases Driving the Future of Biotech, Pharma and Med-Tech Development cites approximately 200 cases. More than 40 reference tools are included and expert guidance from industry insiders is conveyed to give the reader the information that can make the difference in avoiding the “worst-case scenario.”

For more information, please call our customer service department at (800) 688-2421 or (404) 262-5476 or go to www.BioWorld.com.

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