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The following guideline can be ordered through the address listed in the "Source/Publisher"-category.
In cases in which you can order through the Internet we have established a hyperlink.
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| Validation-Master Plan, IQ, OQ, non-sterile Process Validation, Cleaning Validation (PI 006-3) Sept 2007 |
| Short Title: | PI 006-3 |
| Internet: | http://www.picscheme.org/publication.php?download&file=cGktMDA2LTMtcmVjb21tZW5kYXRpb24tb24tdmFsaWRhdGlvbi1tYXN0ZXItcGxhbi5wZGY_ |
| Origin/Publisher: | Secretariat of the Pharmaceutical Inspection Convention c/o EFTA Secretariat 9-11, rue de Varembé, CH - 1211 Geneva 20, http://www.picscheme.org |
| Content: | This document comprises individual Recommendations on four topics relating to Equipment Qualification and Process Validation in pharmaceutical manufacture, as follows:
Validation Master Plan
Installation and Operational Qualification
Non-Sterile Process Validation
Cleaning Validation
The four Recommendations comprising this document define general principles pertaining to each of the topics. |
| Document Type: | Recommendation |
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