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All Updates
- FIFO list of Class A,B,C,D Medical Devices for ImportJune 24, 2025
- Call for applications for financial grants under the central research fund DRAPJune 24, 2025
- Guidelines for conduct and reporting of good clinical practice inspectionsJune 23, 2025
- Recall Alert: RECALL OF PRODUCTS CONTAINING HYDROXYPROGESTERONE CAPROATEJune 23, 2025
- Rapid Alert: CRACKDOWN AGAINST FALSIFIED / SPURIOUS DRUGSJune 23, 2025
- Disposal of Import cases of Alternative Medicines with short shelf lifeJune 20, 2025
- Recall Alert: Recall of Substandard “Tovir 0.5mg Tablet” Batch No. 55, Manufactured by M/s Adamjee Pharmaceuticals (Pvt.) Ltd, Karachi.June 19, 2025
- Guidance on Emergency Use AuthorizationJune 17, 2025
- Date wise provisional list of applications for provisional enlistment of herbal,Homeo,Neutraceutical products applied by nutraceutical firmsJune 13, 2025
- Amendment in the Drugs (Licensing, Registering and Advertising) Rules, 1976 (S.R.O 1047(I)/2025)June 11, 2025
- Amendment in Medical Devices Rules, 2017 (S.R.O 1049(I)/2025)June 11, 2025
- Recall Alert: PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIESJune 10, 2025
- MINUTES OF 57TH MEETING OF CLINICAL STUDIES COMMITTEE HELD ON 20th MAY, 2025.June 5, 2025
- Bidding Document for Provisioning of Electronic Payment Gateway (EPG)
Services to Drug Regulatory Authority of PakistanJune 5, 2025 - Priority Processing of Mexiletine & Systeamine Registration ApplicationJune 5, 2025
- Recall Alert: PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIESJune 2, 2025
- Minutes of the 347th Meeting of the Registration Board Held on 28th – 30th APRIL, 2025June 2, 2025
- Pharmacovigilance NewsletterJune 2, 2025
- Recall Alert: RECALL OF XARELTO 15MG TABLET, BATCH NO. BXK4E11, DUE TO A LABELING ERROR ON SECONDARY PACKAGINGMay 23, 2025
- Rapid Alert: CRACKDOWN AGAINST FALSIFIED/SPURIOUS DRUGSMay 22, 2025
- Stakeholders are invited to comment on Draft Guidelines on Emergency Use Authorization by 06th June, 2025May 22, 2025
- Training Session on MDMC Licensing and Product Registration Portal on: https://www.facebook.com/OfficialDRAP/May 21, 2025
- Comments are invited on revision of Guidelines on Inspection of Good Clinical Practices for Clinical TrialsMay 21, 2025
- Stakeholders Comments are invited on revision of Guidelines for Conduct of Clinical Research in PakistanMay 21, 2025
- Minutes of the 346th Meeting of the Registration Board Held on 22nd April, 2025May 21, 2025
- Rapid Alert: CRACKDOWN AGAINST FALSIFIED/SPURIOUS DRUGSMay 19, 2025
- Training of online CPI module for submission of applications(Wednesday May 21, 10:30 AM)May 19, 2025
- Minutes of 305th Meeting of the Central Licensing Board held on 24th January, 2025May 13, 2025
- Minutes of 302nd Meeting of the Central Licensing Board held on 20th November, 2024May 13, 2025
- Tender Notice for Supply & Installation of Air Conditioners, Led Tv, Multimedia Screens and Projector in DRAP HQMay 8, 2025
- Recall Alert: PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIESMay 7, 2025
- Recall Alert: PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIESMay 7, 2025
- Minutes of the 345th Meeting of the Registration Board Held on 19th to 21st February, 2025May 5, 2025
- Rapid Alert: PRESENCE OF FALSIFIED INJECTION RHOPHYLAC 300MCG, HUMAN ANTI-D IMMUNOGLOBULIN PURPORTEDLY MANUFACTURED BY M/S. CSL BEHRING AG, SWITZERLANDApril 30, 2025
- Decisions of 88th Meeting of the Medical Device BoardApril 28, 2025
- Decisions of 87th Meeting of the Medical Device BoardApril 28, 2025
- Decisions of 86th Meeting of the Medical Device BoardApril 28, 2025
- Decisions of 85th Meeting of the Medical Device BoardApril 28, 2025
- Potential Risk of Tumour Lysis Syndrome with SorafenibApril 25, 2025
- Safety Alert of Risk of persistent corneal injury and significant visual impairment with Chlorhexidine (cutaneous use)April 25, 2025
- Recall Alert: SUBSTANDARD PRODUCTS DECLARED BY DRUG TESTING LABORATORIES.April 25, 2025
- Expressions of Interest (EOI) for shortlisting of expert members of Central Licensing Board of DRAPApril 24, 2025
- Prequalification Document for Vendors/Firms through EPADS for the Supply of Services for Repair & Maintenance WorkApril 24, 2025
- Decisions of 78th Meeting of the Medical Device BoardApril 23, 2025
- Rapid Alert: CRACKDOWN AGAINST FALSIFIED / SPURIOUS DRUGSApril 22, 2025
- DRAP-PSW Gateway: Online application for Pharmaceutical export certificatesApril 21, 2025
- Bidding Document for Appointment of Tax ConsultantApril 21, 2025
- ADVISORY TO THERAPEUTIC GOODS MANUFACTURERS: MEASURES TO PREVENT DEG/EG CONTAMINATION IN ORAL LIQUID PREPARATIONSApril 21, 2025
- MDMC Data List (Local)April 21, 2025
- MDMC Data List (Import)April 21, 2025
