Dear Madam,
Greetings!
I’m Gayan, working as a regulatory affairs officer at the Medmart pharma. We have to plan to start our business with your company. We are interesting your cosmetics product range. One month ago, Mr.Nuwan Fonseka (Director-Medmart Pharma) met authorized person (Ms. Ivonne) from your company during his visit to Cuba. But after he came to Sri Lanka, We couldn’t contact that person so far.
We want to initiate a business relationship with your company.
For the registration of this product in NMRA, Sri Lanka (National Medicines Regulatory Authority) kindly let us know the availability of following documents.
1. COPP
2. GMP
3. Manufacturing Licence
4. Stability Reports (Real Time and Accelerated)
5. Finished Product Test reports
6. Clinical Trial Data
We would like to know following details for our information also.
1. Composition of the product
2. Label or PIL of the product
3. Shelf Life
4. Availability Registration certificate issued by manufacturing country
5. Availability of Registration certificates from foreign countries
Awaiting your reply.
Best Regards
Gayan
Gayan Thilina Amarasinghe B.Pharm
Executive – Regulatory Affairs
Mob: +***