When selecting a pharmaceutical manufacturing partner, choosing a WHO-GMP certified pharma company in India is a smart move toward quality, compliance, and global competitiveness. WHO-GMP certification (World Health Organization – Good Manufacturing Practices) is an assurance that the manufacturer meets international standards in hygiene, documentation, production processes, and quality control.
What to Look for in a WHO-GMP Certified Manufacturer
Choosing the right WHO-GMP certified manufacturer involves careful assessment of:
- Certification Validity: Check if the WHO-GMP certificate is up-to-date and issued by the authorized local body.
- Experience & Track Record: Look for a company with a strong legacy of serving domestic and international clients. Learn about our journey here.
- Product Range: Ensure the manufacturer handles the type of formulations you require (e.g., tablets, injectables, syrups, etc.).
- Regulatory Expertise: A competent partner should also offer regulatory documentation for export markets.
Compliance, Quality Control & Batch Records
A hallmark of a trusted WHO-GMP certified pharma company in India is strict adherence to GMP documentation:
- Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR)
- Real-time quality checks during production
- Validated equipment and calibration logs
- Audit trails and data integrity in every step
These elements ensure not only product quality but also accountability for every unit produced.
Infrastructure Standards Set by WHO
According to WHO-GMP norms, the manufacturing infrastructure must meet specific requirements, such as:
- Hygienic and cleanroom-compliant environments
- Separate zones for different formulations to avoid cross-contamination
- Effluent and waste management systems
- HVAC systems for air purification
Tanishq Lifecare’s manufacturing facility meets and exceeds these requirements, making it ideal for third-party and private-label clients.
Why Tanishq Lifecare is a Trusted Choice
As a WHO-GMP certified pharma company in India, Tanishq Lifecare stands apart due to:
- Over two decades of manufacturing excellence
- WHO-GMP, ISO 9001:2015, and DCGI certifications
- End-to-end contract manufacturing services
- Regulatory support for domestic and international clients
We empower businesses to launch and scale with confidence. Explore our WHO-GMP services.
Ready to partner with a trusted WHO-GMP certified manufacturer? Contact us now.
Frequently Asked Questions (FAQs)
1. How can I verify a WHO-GMP certified pharma company in India?
To verify, ask the company for a copy of their WHO-GMP certificate and check the issuing authority. You can also verify with local FDAs or check whether the facility is listed on official regulatory websites.
2. Does WHO-GMP ensure product safety and regulatory readiness?
Yes. WHO-GMP compliance covers hygiene, process controls, validation, and documentation—key factors for safety and global market approvals.
3. What role does documentation play in WHO-GMP pharma manufacturing?
Documentation ensures traceability, accountability, and audit readiness. It includes SOPs, equipment logs, batch records, and quality testing reports. This is critical for regulatory audits and international trade.