GMP Licence
Ensure Quality & Regulatory Compliance with GMP Certification
The GMP (Good Manufacturing Practices) Licence is a mandatory certification for businesses involved in the manufacturing of food, pharmaceuticals, cosmetics, medical devices, and certain other products. Issued under the Drugs and Cosmetics Act, 1940 or by FSSAI depending on the product category, GMP certification ensures that manufacturing facilities follow strict hygiene, safety, and quality standards.
At Induce India, we offer expert consultation to help manufacturers, exporters, and pharmaceutical companies obtain GMP certification efficiently, enabling them to meet Indian and international compliance standards.
What is GMP Certification?
Good Manufacturing Practices (GMP) are a set of quality assurance guidelines that ensure products are consistently produced and controlled according to quality standards. The objective is to minimize risks involved in production that cannot be eliminated through testing the final product alone.
GMP Licence is essential for:
- Pharmaceutical manufacturers
- Nutraceutical and supplement companies
- Cosmetic product manufacturers
- Medical device and surgical equipment producers
- Herbal and Ayurvedic product manufacturers
- Food processing and packaging units
Why is GMP Certification Important?
GMP Licence Issuing Authorities
- For Pharmaceuticals: State Drug Control Department under CDSCO
- For Food Products: FSSAI (under FSS Regulations, 2011)
- For Ayurvedic/Herbal Products: AYUSH Department
- For Cosmetics and Devices: State FDA or CDSCO (as per product type)
Process for Obtaining GMP Licence
-
Gap Assessment & Documentation Support
We evaluate your current facility and processes to identify gaps and assist in preparing SOPs, QA/QC records, and documentation as per GMP standards. -
Application Filing
Submission of application with supporting documents to the relevant authority (CDSCO, FSSAI, AYUSH, etc.). -
Facility Inspection
Inspection by regulatory officers to assess hygiene, quality control, documentation, equipment calibration, staff training, and storage facilities. -
GMP Licence Grant
Upon successful inspection and document verification, the GMP certificate is issued. Validity ranges from 1 to 3 years depending on the authority.
Documents Required for GMP Certification
- Manufacturing site layout plan
- Proof of ownership/lease of premises
- List of equipment and machinery
- SOPs and QA/QC procedures
- Water & environmental monitoring records
- Details of technical staff and their qualifications
- Copy of drug/food/cosmetic manufacturing licence (if applicable)
- Product list and formulations
Benefits of GMP Certification
- Legal authorization to manufacture and sell regulated products
- Recognition in global markets (WHO-GMP helps in exports)
- Improved operational efficiency and product quality
- Reduction in contamination, errors, and customer complaints
- Enhanced credibility for private label or B2B partnerships
Who Needs a GMP Licence?
- Medicine and pharmaceutical manufacturers
- Cosmetic and personal care product producers
- Ayurvedic, Unani & Siddha product manufacturers
- Dietary supplement and nutraceutical companies
- Food & beverage manufacturers and exporters
- Medical equipment and device producers
Why Choose Induce India for GMP Licence Consultation?
- In-depth expertise in CDSCO, FSSAI, and AYUSH regulations
- Assistance in preparing GMP-compliant documentation
- On-site support for facility audit readiness
- Quick turnaround time and hassle-free certification
- Post-certification assistance with renewals and upgrades (WHO-GMP, ISO, etc.)
Apply for GMP Licence with Induce India Today
Whether you're launching a new facility or scaling for export, Induce India ensures you obtain your GMP certificate with full regulatory compliance. Let our team help you achieve certification success with minimal effort and maximum impact.