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About Active Pharmaceutical Ingredients Development Manufacturing and Regulation
Focusing on the three most critical components that successfully bring an API to market-process development, manufacturing, and governmental regulation and approval-this reference serves as a step-by-step guide to the planning and clear understanding of the bulk manufacturing of APIs. This guide offers current and timely discussions of the process development cycle, design engineering, the approval process, quality control and assurance, and validation, as well as plant manufacturing activities including materials management, maintenance, and safety.
Detailed Information
| Author: | Stanley Nusim |
|---|---|
| Publication Year: | 2005 |
| Pages: | 341 |
| Language: | English |
| File Size: | 8.666 |
| Format: | |
| Price: | FREE |
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