03 June 2019 | News
The GLP certificate from National Good Laboratory Practice Compliance Monitoring Authority opens up the opportunity for Cadila Pharmaceuticals
Cadila Pharma recently received the Good Laboratory Practices Certification from National Good Laboratory Practice (GLP) compliance Monitoring Authority (NGCMA), Dept. of Science and Technology, Govt. of India, for their Pre-Clinical Department after an inspection was held from 4th to 6th February 2019. This certificate is for Dholka facility which is capable of conducting toxicity studies, mutagenicity studies, and analytical and clinical testing. Certificate no. GLP/C-135/2019 was issued on 6th May 2019.
GLP is a data-driven system that establishes the use of industrial chemicals, pharmaceuticals, veterinary drugs, pesticides, cosmetic products, food products, feed additives products, etc. do not pose any hazards to human health and the environment.
The inspection includes:
Breaking the news Mr. Chintan Patel, Head Pre-Clinical & Innovation Team at Cadila Pharmaceuticals Ltd quoted “We are unique in a way where we can say we are ‘One stop solution’ and in pre-clinical research we do offer our pharma research experience and expertise for basic research as well as regulatory studies.”
"With this milestone we are a GLP compliant facility, our regulatory research dossier will have an acceptance in all OECD member countries (>35).Also an additional support to offer services from NCE synthesis to clinical trials is added advantage for contracting R&D.”