1.0 OBJECTIVE To define the standard entry procedure for personnel into the manufacturing corridor of the oral solid dosage (OSD) area to prevent contamination, mix-ups and to maintain GMP. 2.0 SCOPE This procedure is applicable to all personnel (Production, QA,…
1.0 OBJECTIVE To lay down the procedure for safe and GMP-compliant operation of the Vibro Sifter used for sifting of raw materials, granules and blends in the pharmaceutical manufacturing area. 2.0 SCOPE This SOP is applicable to all vibro sifters…
1.0 PURPOSE To define the procedure for GMP-compliant dispensing (weighing) of raw materials for manufacturing, ensuring correct identity, quantity, status and traceability. 2.0 SCOPE Applicable to all raw materials (API + excipients) dispensed for oral solid dosage manufacturing in the…
1. Regulatory background – why this notification came India has now translated this into binding pharmacopoeial and regulatory requirements. 2. What the Indian Pharmacopoeia amendment says (Oral Liquids) Indian Pharmacopoeia (IP) 2022 – Amendment List 09 (10 Oct 2025): 3.…
1.0 Objective: To describe the procedure for analyzing and identifying gases formed in the blister cavities of Amoxicillin and Potassium Clavulanate tablets using Gas Chromatography (GC). 2.0 Scope: This SOP applies to the analysis of gases collected from bulged or…