GMP: EMA Reflection Paper on Sourcing Biological Starting Materials
08.03.2012
After the FDA has recently published a draft Guidance on Monitoring Crude Heparin for Quality, the European Medicines Agency EMA has now drafted a Reflection Paper on the use of starting materials and intermediates collected from different sources in the manufacturing of biological medicinal products.
The source of the news: http://www.gmp-compliance.org/eca_news_3025_7191,7360.html
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