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EU Medical Device Regulation 2017/745
GMP Publications Quality Compliance Publications Helping Companies Meet and Exceed FDA and Total Quality Management Standards
o Combination Product Master Handbook
ICH Q7 GMPs for Active Pharmaceutical Ingredients
Electronic Signatures:
ICH Q7, Q8(R2), Q9(R1), Q10 and Q11 1271 EU Medical Device Regulation 2017/745International Conference on Harmonisation Regulations ICH Q7 GMP Guide for Active Pharmaceutical Ingredients ICH Q8(R2) Pharmaceutical Development ICH Q9(R1) Quality Risk Management ICH Q10 Pharmaceutical Quality System ICH Q11 Development and Manufacture of Drug Substances (Chemical Entities and Biotechnological Biological Entities)
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US$ 570.00
