Storage of Medicinal Products
Correctly Implementing GMP and GDP Requirements
Current regulatory requirements and their implementation in practice
1st edition 2019
Delivery immediately after receipt of payment
Excerpt from the GMP Compliance Adviser
The quality of finished medicinal products and their starting materials must not be adversely affected during storage. This basic requirement of the GMP regulations constitutes a great challenge. Substance changes, contaminations and mix-ups are known and common risks.
This pharma guide explains the current regulatory requirements for storage of medicinal products and describes their implementation in practice. You will learn which requirements the premises must meet and how you can ensure the required storage conditions.
GMP-critical aspects in connection with material handling, warehouse organisation and goods receipt are also discussed. A detailed case study provides risk-based concepts for storage at room temperature and challenges conventional limits. The study investigates the question: What is the point of "heating" medicinal products to 15–25 °C?
The e-book also addresses:
- Storage organisation
- Storage areas
- Storage conditions
- Incoming goods
- Standard storage at 15–25 °C?
Order now your copy of Storage of Medicinal Products – Correctly Implementing GMP and GDP Requirements!
Reading Sample "Storage of Medicinal Products"
- Pharmaceutical manufacturers
- Logistics providers
- Responsibles for warehousing, monitoring and hygiene
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Filesize: 14,45 MB
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