Storage of products at Behansar Active Pharmaceutical Ingredient (API) Manufacturing Plant is a critical stage within the quality chain and must be carried out in full compliance with GMP requirements. This process includes the physical segregation and proper identification of raw materials, packaging materials, in-process materials, and finished products. Warehouse environmental conditions—such as temperature, humidity, light exposure, and cleanliness—must be continuously monitored and documented to ensure product quality and stability.

All materials must be clearly labeled with information including name, code, batch number, quality status (quarantine, approved, or rejected), and expiry date. Adherence to FIFO/FEFO principles, prevention of cross-contamination, control and prevention of pest and vermin ingress, securing access points, sealing and routine inspections, personnel access control, availability of written standard operating procedures (SOPs), and full traceability of each batch up to its final destination are essential requirements for storage in an API manufacturing facility.