UNCOMPROMISING
QUALITY STANDARDS
Every softgel capsule manufactured at our WHO-GMP certified Haryana facility undergoes rigorous quality control -- from raw material testing to final dispatch.
Food Safety and Standards Authority of India
Compliance with India's food safety and quality regulations for manufacturing and distribution of food products.
Good Manufacturing Practice
Adherence to internationally recognized manufacturing standards ensuring product quality, consistency, and safety.
Hazard Analysis and Critical Control Points
Systematic approach to food safety that identifies, evaluates, and controls hazards throughout production.
Halal Certification
Products manufactured in compliance with Islamic dietary requirements, expanding market accessibility globally.
World Health Organization GMP
Meeting WHO standards for nutraceutical manufacturing, recognized by regulatory bodies worldwide.
Our facility is certified by FSSAI and other regulatory bodies. Additional certifications and documentation available on request.
MULTI-POINT QUALITY CHECKS
Our in-house quality control laboratory is equipped for comprehensive testing at every stage of production - from incoming raw materials to finished product release.
- 01Raw material identity and purity testing
- 02In-process weight and fill volume checks
- 03Dissolution and disintegration testing
- 04Microbial limit testing
- 05Stability testing under controlled conditions
- 06Finished product visual inspection
- 07Batch documentation and traceability
- 08Packaging integrity verification
Batch Testing
Every single batch is tested and documented before release - no exceptions.
QUALITY & CERTIFICATIONS Q&A
01What testing does each batch undergo?
Every batch is subjected to a multi-point quality control protocol: raw material identity and purity testing, in-process weight and fill volume checks, dissolution and disintegration testing, microbial limit testing, finished product visual inspection, packaging integrity verification, and full batch documentation. No batch leaves our facility without passing all checks.
02Will I receive a Certificate of Analysis (COA) with my order?
Yes. A Certificate of Analysis is provided with every batch, documenting test results for active ingredients, microbial limits, dissolution profile, and physical specifications. Additional regulatory paperwork (Free Sale Certificate, ingredient declarations, etc.) is available on request for export shipments.
03Can I audit your manufacturing facility?
Yes — we welcome scheduled facility audits from prospective partners, distributors, and certification bodies. Visits are typically arranged within 1–2 weeks of an audit request. Contact us at team@admetuslifesciences.com to schedule.
04What certifications does Admetus Lifesciences hold?
Our facility is FSSAI, GMP, HACCP, Halal, and WHO-GMP certified. Certificate copies and audit reports are available for qualified business inquiries to support partner due diligence and export documentation.
05How long are products stable, and is stability testing performed?
Stability testing is performed under controlled temperature and humidity conditions to validate shelf life claims. Specific shelf life depends on the formulation and packaging — typical shelf life for our softgel capsules ranges from 24 to 36 months. Stability data is available for each formulation on request.
06Do you provide third-party lab testing or only in-house QC?
Our in-house QC laboratory handles routine batch testing. For specialized assays, regulatory submissions, or validation studies, we coordinate with NABL-accredited third-party laboratories. Results from third-party testing are shared with the relevant batch documentation.
REQUEST QUALITY DOCUMENTATION
Certificate copies, audit reports, and compliance documentation are available for qualified business enquiries.
Request Documentation