Manufacturing

TANISHQ has entered into lease/license agreements with state of the art manufacturing sites for production of its products. All Plants have infrastructure to handle Global Pharmaceutical requirements. The manufacturing is done as per technical specifications of Tanishq with best quality and confirming to stringent international standards.

Tanishq cares about modern Quality Control for API / PM, Finished Products which ensures that our products are pure, safe and effective and are released only after thorough analysis as per stringent specifications, methods and procedures developed according to international guidelines.

Since its establishment, Tanishq has maintained the highest standards of quality control and assurance adhering to the self-enunciated SOPs (Standard Operating Procedures) for efficient and hazard-free operations. We at Tanishq Life Care always oblige to manufacture products which fulfill the desires of mankind & provide them full product satisfaction.

We adjust and adapt to the changing needs of our customers and remain dedicated in our efforts to serve them to the best of our ability. Against all odds, we must strive to follow the cGMP guidelines as described by WHO to ensure the quality of products we manufacture. We work together to bring in health and happiness to enhance the quality of life.

"WE ARE COMMITTED TO ACHIEVE EXCELLENCE IN QUALITY STANDARDS AND ALWAYS SUPPLY PRODUCTS AS PER GLOBAL REQUIREMENTS"
Regulatory Affairs & Documentations

We have a highly skilled team of regulatory affairs specialists who are well versed with regulatory policies and procedures around the world. They have a wealth of experience in the timely filing of dossiers as well as handling regulatory queries from both authorities and customers. Tanishq’s regulatory team is well experienced in developing dossiers as per CTD/ACTD formats for such complex products. Tanishq has a distinguished regulatory department specifically for DCGI & FSSAI approvals.

The department in co-ordination New Product Development Team work towards the needs and wants of the business partners. The Bio-Equivalence studies & Clinical Trials are also arranged by the said department as and when asked by DCGI.

Regulatory Affairs & Documentations

We have a highly skilled team of regulatory affairs specialists who are well versed with regulatory policies and procedures around the world. They have a wealth of experience in the timely filing of dossiers as well as handling regulatory queries from both authorities and customers. Tanishq’s regulatory team is well experienced in developing dossiers as per CTD/ACTD formats for such complex products. Tanishq has a distinguished regulatory department specifically for DCGI & FSSAI approvals.

The department in co-ordination New Product Development Team work towards the needs and wants of the business partners.The Bio-Equivalence studies & Clinical Trials are also arranged by the said department as and when asked by DCGI.