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About Global Medical Device Regulatory Strategy Second Edition Toc
This document provides an overview of 22 chapters focused on developing regulatory strategies for medical devices on a global scale. The chapters cover topics such as developing core teams, regulatory basics, quality management systems, risk management, labeling strategies, nonclinical testing, clinical strategies, combination products, global regulatory processes, use of standards, marketing strategies, and more. The document is intended to provide guidance to medical device companies on the various regulatory considerations involved in bringing products to markets around the world.
Detailed Information
| Author: | ['harshit'] |
|---|---|
| Publication Year: | 2023 |
| Pages: | 4 |
| Language: | English |
| Format: | |
| Price: | FREE |
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