We offer complete sourcing and & supply chain management to our clients from development to commercial phase. In addition we also offer NCE development, Process development and improvements where required. The company offers representation to API companies intending to register and sell their products into India.
From Development upto commercial supplies we are experienced in project management, licensing, manufacturing, CMO, and supply chain. We work with reliable supply partners on long term associations that ensure planned and predictable outputs.
Where required by clients, thro our partner CRO’s offer Clinical, BA/BE studies, Population studies, Toxicology studies and summary reports where required. The experts are associates of the company.
We offer Audits of facilities for GMP compliance and continuous monitoring. Our associates are qualified adequately to assure our clients on the cGMP status with specific references i.e FDA, EDQM, ICH, TGA etc.
Supporting these is also a team of Regulatory Affairs personnel who are competent to review documents that qualify for internal compliance as well as submission to regulatory agencies worldwide.
Specific business opportunities for intermediate chemicals for API manufacturing, Excipients and packaging materials are offered on engagement.
Strategic deals & acquisitions and identifying potential targets for such transactions are offered by us.
RLD’s for generic or clinical development can be arranged by us.