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GRRMDP

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

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Ms. Prema Desai

Ms. Bharathi Ramesh

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ICH Q1

Guidelines on pre-market approvals requirements-

STABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS Q1A(R2)

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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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