Good Manufacturing Practices as per World Health Organization standards. The gold standard for pharmaceutical quality.
Our experts will call you within 30 minutes to discuss your requirements.
WHO Good Manufacturing Practice (GMP) guidelines are designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
Comprehensive audit of manufacturing facilities and processes.
POPULARImplementation of robust testing and documentation protocols.
RECOMMENDEDStructural and operational validation as per WHO norms.
FAST-TRACKA curated list of requirements for a hassle-free registration process.
Copy of valid drug manufacturing license from state authority.
Complete SMF containing plant layout and equipment details.
Details of technical staff and their qualifications.
Water system, HVAC, and process validation reports.
Initial assessment of the plant and documentation status.
Gap analysis and setting up SOPs as per WHO norms.
Final inspection by the regulatory body or auditors.
Issuance of WHO-GMP Certificate upon compliance.
Direct access to Senior CAs and CS experts throughout the registration process.
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Premium quality service at the most competitive and transparent prices.