After tablets and capsules are manufactured, they undergo rigorous quality control testing to confirm they meet the required specifications. Tests are conducted to assess assay, physical parameters, hardness, disintegration time, dissolution rate and uniformity of content. Only tablets and capsules that pass these tests are released for distribution.
Tests are conducted to assess a tablet's assay, physical parameters, hardness, disintegration time, dissolution rate and uniformity of content. Only tablets and capsules that pass these tests are released for distribution.
A dedicated, fully equipped microbiology laboratory is available for comprehensive environmental and utility control, including routine purified-water testing, environmental monitoring (EM), drain sanitation checks, and compressed-air validation. The laboratory plays a vital role in raw-material component analysis and finished-drug-product testing, ensuring absolute microbial contamination control prior to release.
Equipped with the latest research equipment — HPLC, UV spectrophotometer, FTIR, dissolution apparatus, potentiometer, bio-safety cabinet and laminar air flow — our laboratory's analytical testing procedures conform to IP, BP, USP and other official compendia, as well as in-house specifications that surpass various pharmacopoeia standards.
Analytical testing conforming to IP, BP, USP and other official compendia.
Raw-material and finished-product characterisation ahead of every release.
Dedicated microbiological testing ahead of nationwide and export release.
Sai Sarvaa focuses its quality on all areas — from procuring raw materials and applying the best manufacturing technology, to functional operations, timely delivery of formulations, and promotional support for building a product brand. This ensures swift access into nationwide domestic markets. Our Research and Development team is led by proficient chemists, scientists and technicians.
A set of qualified persons manage the Quality Assurance department. They constantly examine the quality of the products by performing systematic testing and sampling at each stage, from raw materials until completed pharmaceutical formulations. WHO-cGMP standards are followed throughout, and we integrate up-to-date testing equipment to perform strict, pharmacopoeia-compliant quality analysis.
Issued by Department of Food Safety and Drugs Control Administration, Government of Tamil Nadu, certifying that our site complies with Good Manufacturing Practices as per WHO norms for tablets and hard gelatin capsules — both General and Beta-Lactam categories.
| Certificate No. | TN/WHO/00049 |
|---|---|
| Valid Until | 01/04/2029 |