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GRRMDP

Global Regulatory requirements for Good Manufacturing and Distribution practices in Pharmaceutical /Biopharma industries

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Ms. Bharathi Ramesh

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ICH Q12

Guidelines on pre-market approvals requirements-

Q12_Annexes_ICH

Q12_Guideline_ICH

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Thanks to Dr. Kirti Kulkarni for the compilation of PDF formats of all guidelines along with Ms. Prema Desai. © All Rights Reserved 2023-2035 - Fully Illustrated by Arpita Sathyanarayanan

(https://in.linkedin.com/in/arpita-sathya).

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