You Spent years developing the product

You Can’t Afford to wait long enough to VALIDATE

Whether you are subjected to regulatory body audits such as WHO (Schedule M), WHO (Geneva), TGA, USFDA, MHRA, MCC, ENVISA, we can help you with entire validation requirements for complying with GMP, cGMP, GAMP 5, 21 CFR Part 11 Software Validation and achieve the right level of Validation and traceability to National and International Standards.

Autocal Solutions Pvt. Ltd offers a full range of Validation services as per the requirements of Industry. These Include
• Development of Protocols; DQ, IQ, OQ &PQ for Equipments and Processes.
• Validation of Sterilisers; Steam, Dry Heat &EO.
• Validation of QC Equipments like Ovens, BODs, Incubators, Stability Chambers, Environmental Chambers, Water
• Baths, Deep Freezers, Etc
• Temperature and / or RH Mappings of Cold Rooms, Warehouse, Control Sample Rooms, Clean Areas.