R & D
D K Pharma has a State-of-the-art Quality Control Department with the latest equipments like IR / GC / HPLC / UV and Karl Fischer.
Also available is in-house Analytical Method Validation for Active Pharmaceutical Ingredients (APIs) and Intermediates.
This Department also makes available in-house Long Term as well as Short Term Stability Studies of products developed.
The Quality Control Department is capable of supporting our Drug Master File.
Intermediates are manufactured and documented as per GMP norms.
The Department is also responsible for Confirmity of Quality of Active Pharmaceutical Ingredients (APIs) for IP, EP, BP, USP, JP as well as CP.
Copyright © 2016. DK Pharmachem All Rights Reserved.
Designed & Developed by: