Certifications & Quality
Every product we manufacture is backed by rigorous quality systems, internationally recognised certifications, and an unwavering commitment to patient safety.
Our Commitment
Quality is Not a Department — It's Our Culture
At Relivia Life Sciences, quality assurance is embedded into every stage of our operations — from raw material sourcing and formulation development to manufacturing, packaging, and distribution. Our quality management system is built on internationally recognised standards and continuously audited to ensure compliance.
4+
International & national certifications
Our Credentials
Certifications & Licences
Our manufacturing facility is certified under WHO Good Manufacturing Practices — the global benchmark for pharmaceutical production. This certification confirms that our processes, facilities, and documentation meet the highest international standards for medicine quality and safety.
How We Maintain Quality
Our Quality Management System
Raw Material Control
Every raw material is sourced from approved vendors and subjected to rigorous identity, purity, and potency testing before entering our manufacturing process.
In-Process Quality Checks
Our QA team conducts systematic in-process checks at every critical stage of manufacturing to detect and prevent deviations before they affect the final product.
Finished Product Testing
Every batch undergoes comprehensive finished product testing — including assay, dissolution, microbial limits, and stability — before release to market.
Stability Studies
We conduct ICH-compliant stability studies for all products to establish shelf life and ensure potency and safety throughout the product's intended use period.
Documentation & Traceability
Complete batch manufacturing records and traceability documentation are maintained for every product, enabling full audit trails from raw material to patient.
Continuous Improvement
We operate a formal CAPA (Corrective and Preventive Action) system, ensuring that any deviation or non-conformance is investigated, resolved, and used to improve our processes.
Regulatory Compliance
Relivia Life Sciences operates in full compliance with the Drugs and Cosmetics Act, 1940, and all applicable rules and regulations issued by the Central Drugs Standard Control Organisation (CDSCO) and State Licensing Authorities. Our products are registered and approved for sale in India, with select products cleared for export to international markets under applicable regulatory frameworks.
Applicable Frameworks
- Drugs and Cosmetics Act, 1940 (India)
- Schedule M — Good Manufacturing Practices
- WHO Technical Report Series — GMP Guidelines
- ICH Q1A–Q1F Stability Guidelines
- ICH Q7 — Active Pharmaceutical Ingredients
Questions About Our Quality Standards?
Our quality assurance team is happy to answer any questions from healthcare professionals, distributors, or regulatory bodies.