Folder Guidance Documents


Toggle Title Download
pdf Guidelines for GMP, Import, Export and Destruction of Investigational Medical Products (IMPs) for Clinical Trials Bangladesh Download
pdf Guidelines on import procedures for medical products Download
pdf Guidelines for Registration of Human Vaccines Download
pdf Final Print BD Stem Cell Guidelines 18 03 2020 Download
pdf Good Storage and Distribution Practices for Medical Products, WHO TRS No. 1025, 2020, Annex 7 Download
pdf Recall Guideline Download
pdf Guidance for industry about Post Licensure Change Download
pdf Guideline on Clinical Evaluation of Vaccines Download
pdf Guideline on Good Manufacturing Practices: Water for Pharmaceutical use.WHO TRS 1033 Annex 3 Download
pdf Guideline on Quality Management System requirements for National Inspectorates.WHO TRS 1025 Annex 5 Download
pdf Guideline on Good manufacturing practices: Guidelines on validation.WHO TRS 1019 Annex 3 Download
pdf Guideline for Post Marketing Authorization Download
pdf Procedure for Expedited Marketing Authorizatio of COVID-19 Vaccines in South-East Asia Region Download
pdf Pharmacovigilance Protocol for Covid 19 Vaccines Download
pdf Guidelines on Good Manufacturing Practices for Biological Products Download
pdf WHO guideline for safe disposal of unwanted pharmaceuticals in and after emergencies Download
pdf Guideline to control of promotion, marketing and advertisement of medical products Download
pdf Guideline on Risk Based Post Marketing Surveillance (RB PMS) of Finished Medicinal Products Download
pdf Guideline for Registration of Bulk and Intermediate product of Medicine for Export Download
pdf Complain Guidelines of DGDA Download

DGDA Notice Board

© 2021 All rights reserved for Directorate General of Drug Administration.

Aushad Bhavan, Mohakhali, Dhaka-1212, Bangladesh

Tel : 8802 9880803, 9880864, 9880897, 9880924, Fax : 8802 9880854, E-mail :

Display Date and Time

  • Last Modified: Sunday 06 March 2022, 10:25:32.