Medopharm being an integrated part of TMPL has proven its presence on global front since last five decades by supplying Quality Medicines across 90+ countries from its State-of-Art manufacturing units.
Beyond its manufacturing capabilities Medopharm has strengthened its activity towards turnkey projects through Consultancy Services and Technical support for green field projects in setting up Manufacturing Units, providing assistance in establishing Quality Management System in line with Stringent Regulatory Authority requirement backed by a team of highly experienced professional.
Medopharm has also created a State-of-Art R&D Centre at Chennai equipped with sophisticated testing instruments and GMP compliant development lab for developing bio equivalent generics supported by over 50 highly qualified scientists and analysts with complete focus on new developments of various dosage forms.
Medopharm offers to undertake any outsource project to support Formulation Development, Technology Transfer and other technical value added services based on requirement.
Areas of Expertise:
- Development of BE compliant Generics for Regulatory Markets.
- Scale up and validation of new products.
- Expert in handling of tricky products and stabilising instable products.
- Have gained expertise in development of Immediate release, Sustained Release formulations, effervescence formulations, enteric coated products, Direct Compression Technology, Chewable tablets, Mouth dissolving tablets, etc.