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Welcome to Pharmaceutical Blog

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Guidelines
Method of Analysis (MOA)
Microbiology
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Validation

SCHEDUE M-I

SCHEDUE M-I

pharmablog.in / Guidelines / March 1, 2024 / GMP, SCHEDUE M-I

Good Manufacturing Practices and Requirements of Premises, Plant and Equipment for Homoeopathic Medicines

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Guidelines
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Microbiology
Packaging Material
Quality Assurance
Quality control
SOP
Validation

Site Master File – EU GMP
21 CFR Part 211-cGMP
Spectral Transmission for Colored Glass Containers
Arsenic Test For Glass Container – USP
Surface Etching Test – USP

Mr. Shaikh is the professional pharmaceuticals blogger, founder and author of PharmaBlog.in

Site Master File – EU GMP
21 CFR Part 211-cGMP
Spectral Transmission for Colored Glass Containers
Arsenic Test For Glass Container – USP
Surface Etching Test – USP

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