Our innovative R&D Center conforms to international quality standards and houses advanced and up to date equipment. It has one of the most advanced infrastructures for both basic and applied research. Design of experiments (DOE) and statistical analysis have been applied widely to formulation development, and are useful in formula and process optimization.
TIZIG Pharmaceuticals has dedicated teams of highly qualified scientists working on patent navigation, specializes in creating alternate and patentable processes for generic formulations, process development, scaling-up, tech transfer and registration of generic products with eCTD dossiers.
Our analytical development team capable to develop methods of analysis lay down specifications and work out quality assurance norms in relation to all the above activities. The R&D facility is geared toward development of technologically challenging products. We strive to develop cost-effective, high-quality formulations to make the life of the patient better.
TIZIG Pharmaceuticals has a well-planned infrastructure with dedicated and segregated blocks for oral dosages and parenteral dosages. Our manufacturing facilities are capable of manufacturing a broad range of Dosage forms. Manufacturing Pharmaceuticals with effective quality management is of paramount importance to TIZIG success. Our manufacturing sites are all regularly evaluated internally and inspected by regulatory authorities to ensure that finished products have the desired identity, strength, quality and purity.