Standard Solutions online (1)
Found iron particles in mebendazole (3)
Elemental Impurities (1)
Compression question (1)
Cleaning validation (1)
Load patterns for sterilization (11)
MHRA and USFDA audit (5)
Disinfectant to be used in API (5)
Difference of FPD and FPF (2)
Material transferrig procedure (4)
Cleanrooms Classification and validation (1)
Sterilization guidelines (3)
Steam generation (1)
Regulatory Inspection Report (of USFDA or EU /MHRA) for Finished product manufacturing site (1)
Pharma code and about 2D Barcode (2)
Overages to compensate loss on storage (2)
NeedFranchise manufacturing with FDA approved pharmaceutical factory (2)
Tablet coating problem (13)
Can anyone help me regarding guidelines required for designing Solvent yard for Class A types solvents(drums) in a shed including vehicle unloading and loading (1)
Lag time and equilibrium time in autoclave (13)
Sop for inprocess and finished products samples (1)
Impact Assessment Report (2)
How many types of cleaning validation (5)
Storage Condition of bulk products (3)
Leak test refernce (2)
Good documentation (6)
Raw material adding procedure for Tablet (8)
Requirement of daily weight checking (16)
Sensors used in compression machine (2)
Friability of Tablets (7)