Unwavering Commitment to Quality
Adhering to Global Standards for Every Formulation. Our rigorous quality systems ensure that every product meets the highest standards of safety and efficacy.
Quality is Non-Negotiable
At SIBR Lifescience, quality is not just a department—it's embedded in our DNA. Every decision we make, from sourcing raw materials to final product release, is guided by our patient-first approach. We understand that behind every product is a patient who trusts us with their health and well-being.
Our commitment to quality goes beyond regulatory compliance. We continuously invest in advanced testing equipment, train our personnel to the highest standards, and implement robust quality management systems that exceed industry requirements.
Recognized Quality Standards
Our manufacturing facility holds multiple certifications demonstrating our commitment to pharmaceutical excellence.
GMP Certified
Good Manufacturing PracticeOur facility meets stringent GMP requirements ensuring consistent production and quality control.
ISO 9001:2015
Quality Management SystemCertified quality management system ensuring continuous improvement and customer satisfaction.
WHO-GMP
World Health Organization StandardsCompliance with international WHO guidelines for pharmaceutical manufacturing.
FSSAI
Food Safety Standards AuthorityLicensed under FSSAI for food supplement and nutraceutical products.
Our QC Process
A systematic approach ensuring quality at every stage of manufacturing.
Raw Material Inspection
Every raw material and API is tested for identity, purity, and potency before acceptance into our manufacturing process.
In-Process Testing
Continuous monitoring during manufacturing ensures each batch meets specifications at every stage of production.
Finished Product Analysis
Comprehensive testing of finished products including assay, dissolution, and microbiological parameters.
Stability Testing
Long-term and accelerated stability studies ensure product quality throughout shelf life.
Release & Documentation
Complete documentation and quality review before batch release for distribution.
Regulatory Vigilance
We maintain continuous vigilance over evolving regulatory landscapes. Our regulatory affairs team stays updated with the latest guidelines from CDSCO, FDA, WHO, and other regulatory bodies to ensure ongoing compliance.
- CDSCO compliance for Indian market
- Regular internal audits and inspections
- Documentation as per Schedule M guidelines
- Pharmacovigilance monitoring
Questions About Our Quality Standards?
We're happy to discuss our quality processes and certifications with healthcare professionals and business partners.