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ISPE Good Practice Guide: Controlled Temperature Chamber Mapping and Monitoring
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Handbook / Manual / Guide by International Society for Pharmaceutical Engineering, 2016
The ISPE Good Practice Guide: Controlled Temperature Chamber Mapping and Monitoring provides industry good manufacturing practices for the temperature mapping of controlled temperature chambers, along with development of test acceptance criteria and a risk-based approach to practices for periodic review of system performance. The approach described is consistent with that described in the ISPE Good Practice Guide: Cold Chain Management.
Guidance is provided on Controlled Temperature Chambers used to store raw material, work in progress, or finished product, and which operate under current Good Manufacturing Practices (cGMPs). A Controlled Temperature Chamber is defined as a system, unit, equipment, or room in which the environmental conditions (usually temperature) of a chamber are controlled, maintained, and regulated to meet specific user requirements.
Types of Controlled Temperature Chambers considered by this guide include:
- Purchased Commercial Off the Shelf (COTS) items (such as freezers, refrigerators, and incubators)
- Warm rooms designed to maintain consistent temperatures
- Ovens, and custom built units, such as controlled room temperature environments, e.g., warehouses, walk-in cold rooms and freezers. Freezers can be used for short to long term preservation of pharmaceutical and biopharmaceutical materials, e.g.:
- Active Pharmaceutical Ingredients (APIs)
- Process intermediates
- Stability samples
- Laboratory materials
- Cell banks
Guidance is provided on the definition of the requirements (producing a user requirements document), design, purchasing, commissioning (including temperature mapping), qualification, and maintenance of controlled temperature chambers operating under cGMPs.
Product Details
- Published:
- 2016
- ISBN(s):
- 9781936379866
- Number of Pages:
- 116
- File Size:
- 1 file , 2.8 MB