DQ, IQ, OQ, and PQ in Pharmaceutical Industry
All pharmaceutical companies are required to abide by stringent regulations to ensure their products are safe and effective. Regulatory authorities specifically emphasize on qualification processes in pharma manufacturing facilities. The process of qualification aims...
20 Key Changes for Ayurvedic Manufacturers in Revised Schedule T Draft
The Schedule T guidelines for ayurvedic medicine manufacturers are being revised to improve the way ayurvedic medicines are manufactured. The aim is to ensure high-quality, safe, and effective ayurvedic medicines are being consistently manufactured. In this blog, we...
GMP and Schedule M Audit Service for Pharmaceutical Facilities
All pharmaceutical manufacturing facilities in India are required to comply with the Schedule M guidelines. The guidelines are intended to change the way pharmaceuticals are manufactured in India bringing them at par with global standards. However, ensuring compliance...