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CAPA Formats- CAPA Request Form & CAPA Register

Corrective Actions and Preventive Actions (CAPA). Download formats from links below- CAPA Request FormDownload CAPA RegisterDownload For any Feedback or suggestion, mail at:

SOP – Good Documentation Practices in Pharma Industry

1.Objective : To lay down a procedure for good documentation practices. 2. Scope: This procedure is applicable to all cGxP documents (electronic & manually generated) used in the manufacturing, packaging, labeling, testing, storage and distribution of Drug...

PIC/S [Pharmaceutical Inspection Convention and Pharmaceutical Inspection Scheme]- Guidelines & Links

                        All    Reference    Category  Section AIDE MEMOIRE ON ASSESSMENT OF QUALITY RISK MANAGEMENT (QRM) IMPLEMENTATION       PI 038-1 Documents for Inspectors Aide-Memoires AIDE MEMOIRE ON GMP PARTICULARITIES FOR CLINICAL TRIAL PRODUCTS        PI 021-2 Documents for Inspectors Aide-Memoires AIDE MEMOIRE ON INSPECTION OF BIOTECH      ...


INTRODUCTION:- The pharmaceutical industry is facing a tremendous changes and challenges nowadays. It has been observed that lack of proficient, talented, capable employees has enforced organization to be innovative in formulating methods to maintain...

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