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Understanding WHO Guidelines for Batch Manufacturing Records

Dot Compliance

The World Health Organization (WHO) has established guidelines for BMRs to ensure consistency, quality, and safety across the global pharmaceutical industry. Dot Compliance includes batch record management capabilities with fast deployment and innovative analytics. Get started now.

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SQA Regulatory Surveillance Summary for May and June 2024

SQA

The establishment’s document control/record management system was not sufficient. The establishment did not always perform a physical exam on the directed donors in accordance with the directive. The establishment did not use appropriate and effective tests for infectious disease testing set out in the directive.

FDA 52
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SQA Regulatory Surveillance Summary for May and June 2024

SQA

The establishments document control/record management system was not sufficient. The establishment did not always perform a physical exam on the directed donors in accordance with the directive. The establishment did not use appropriate and effective tests for infectious disease testing set out in the directive.

FDA 40
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SQA Regulatory Surveillance Summary for January and February 2024

SQA

A health professional, in the context of a directed donation, did not create a document stating that, in their medical opinion, the use of sperm or ova would not pose a serious risk to human health and safety. Now the Ministry of Health has published revised regulations in accordance with Annex M of the Drugs and Cosmetics Rules.

FDA 40