The Drug Regulatory Authority organized a training workshop with financial support from World Health Organisation (WHO), Bhutan at Phuentsholing from 23 October – 3 November, 2017 on Good Manufacturing Practices (GMP). The training workshop was based on PIC/S GMP Guide. The training workshop comprised of 38 participants varying from Regulatory Officials from DRA, Procurement Officer from MSPD, Pharmacists from Drug Testing Laboratory, Quality Control and store personnel from Biological Production Unit (DoL), Menjong Sorig Pharmaceuticals, Neethsel Pharmaceuticals Private Ltd., Aha-Oxy Gases Pvt. Ltd., Quality Gases Pvt. Ltd., Ninjidh Pharmaceuticals Pvt. Ltd and Bhutan Pharmaceuticals Pvt. Ltd. The training workshop was facilitated by Lead Inspector, Bureau of Drug,Thai FDA. The training workshop is expected to enhance the technical capacity of regulators on GMP and make the pharmaceutical manufacturing firms cGMP compliant, thus facilitating availability of quality medicinal products. As a part of the training, on-site GMP Inspection of two Pharmaceutical company was also carried out.