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!

Back to the GMP Shop

Customer reviews can be made anonymously and will be published in our webshop after verification.

Back to the GMP Shop

Pharmaceutical manufacturers
Logistics providers
Responsibles for warehousing, monitoring and hygiene

Back to the GMP Shop

Technical Requirements

This file is in PDF format!
Filesize: 14,45 MB

To view PDF files, we recommend using the Adobe Reader.

Please note the following procedure guidelines:

If you choose payment by bank transfer:

You will receive an advance invoice.
After payment is received an email with the download information will be sent.

If you choose payment by credit card:

Immediately after the credit card payment you will receive an email with the download information.
The invoice will be sent by postal mail as soon as possible.