We are looking for partners in countries where our products are not registered yet or under procedure for registration.

We can offer various formats for registration dossier including:

• Certificate of GMP
• Clinical trials, safety and efficacy study
• Complete Drug formula, Drug literature
• Drug sample, Drug labeling and packaging in English/Local language
• Manufacturing method
• Raw material specifications of actives and inert ingredients with the corresponding control methods in details ( Drug Master File)
• Finished product specification with the corresponding control methods in details
• Certificate of analysis of active ingredient USP/BP
• Drug analytical control
• Stability studies of finished product