We offer manufacturing services for preclinical and phase I clinical trials. We also have DEA license to manufacture controlled substances. Our dedicated production suites operate under cGMP. Our existing facility can produce upto 100000 tablets or 6000 capsules per day. An independent QA monitors all manufacturing and quality control activities, and performs routine upgradation of the following to ensure high standards:

v Review and Approval of Standard Operating Procedures, Batch Production Records, Protocols and Reports.

v In-process quality control, Raw Material - Quarantine and Release, Review and Release of Product.

v Internal and External audits, and Training Programs.

We provide cost competitive solutions, and help advancing your product from bench to bedside. Please contact to know more about us and schedule for an initial meeting.