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All Updates
- 125. Rapid Alert – Crackdown Against Falsified / Spurious/ Unregistered Aphrodisiac Drug Products.December 30, 2025
- 124. Rapid Alert – Crackdown Against Unlicensed / Unauthorized Manufacturers.December 30, 2025
- Requirements for Grant of Drug Manufacturing License by the Way of Basic and Semi-Basic Manufacturing for Blood/Plasma EstablishmentsDecember 29, 2025
- Decisions of the 112th Meeting of the Medical Device Board (MDB) Held on 11-12-2025 (Manual Application – Part II)December 29, 2025
- Minutes of 352nd Meeting of Registration BoardDecember 24, 2025
- Training on software for electronic submission of applications for issuance of Nothing Due Certificate(NDC) on account of central research fund.December 24, 2025
- Training on online module for issuance of CRF-Nothing Due Certificate(NDC) By MIS Division, DRAP (For all pharmaceutical industry)December 23, 2025
- Quota Allocation of Drug Substance for Product Development StudiesDecember 22, 2025
- 123. Recall Alert (Class-I) – Drug Products (Human) Substandard – Gligit Baltistan.December 18, 2025
- 122. Rapid Alert – Falsified / Spurious / Unregistered Tramadol Tablets.December 18, 2025
- 120. Recall Alert (Class-I) – Drug Products (Human) Substandard by DTL Punjab.December 16, 2025
- 119. Recall Alert (Class-II) – Drug Products (Human) Substandard -DTL PunjabDecember 16, 2025
- Decisions of the 110th Meeting of the Medical Device Board (MDB) held on 26-11-2025 & 27-11-2025 (Manual Applications – Part II)December 15, 2025
- Tender for Conducting a National Pharmaceutical Pricing SurveyDecember 14, 2025
- 121. Rapid Alert- Falsified SIMULECT (Basiliximab) for injection identified in the WHO African and European Regions.December 10, 2025
- 118. Recall Alert (Class-I) – DTLs Punjab declared Substandard products (Human)December 8, 2025
- 117. Recall Alert (Class-II) – DTLs Punjab Declared Substandard Drug Products.December 8, 2025
- Decisions of the 108th and 109th Meeting of the Medical Device Board (MDB)December 8, 2025
- Corrigendum of Tender for “Provision & Installation of Shipping Grade Containers for Storage of Record and Prefabricated Guard Cabins”December 3, 2025
- 116. Recall Alert (Class-II)- Drug Products declared Substandard.November 27, 2025
- 115. Recall Alert (Class-I) Veterinary Drug Product declared Substandard.November 27, 2025
- Guideline for Lot Release of Human Vaccines, Blood Products (Plasma-Derived Medicinal Products), and Anti-SeraNovember 27, 2025
- Bidding Document: Provision & Installation of Shipping-Grade Containers & Prefabricated Guard CabinsNovember 21, 2025
- Decisions of the 107th Medical Device Board (MDB) Meeting: Manual Applications (Part II)November 21, 2025
- Decisions of the 106th Medical Device Board (MDB) Meeting: Manual Applications (Part II)November 21, 2025
- 114. Recall Alert (Class-I) – Injection Cyanofar 50ml (Veterinary) – SubstandardNovember 21, 2025
- 113. Recall Alert (Class-I) – Substandard Drug Products (Human)November 20, 2025
- 112. Recall Alert (Class-I) – Veterinary Drug Products (Substamdard)November 18, 2025
- 111. Recall Alert (Class-I) – Veterinary Drug Products (Substandard)November 18, 2025
- 110. Recall Alert (Class-I) – Dexamex Injection (Batch # DX250017)November 17, 2025
- 109. Recall Alert (Class-I) – Zayzine Syrup (Batch # 25289)November 17, 2025
- Training on Software for Electronic Submission of Applications for Quota Allocations and Functions of Controlled Drugs DivisionNovember 14, 2025
- Draft Guideline for Lot Release of Human Vaccines, Blood Products (Plasma Derivatives Medicinal Products) and Anti-Sera (Edition 03)November 13, 2025
- Decisions of the 105th Meeting of the Medical Device Board (MDB) held on 23-10-2025 (Manual Applications)November 13, 2025
- 108. Recall Alert (Veterinary Drug Product) – Melovetz 10 Injection (Batch # 2599063)November 12, 2025
- 107. Recall Alert – (Class-I) Injection Isobaj (Batch # IB-0925)November 12, 2025
- 106.Recall Alert – (Class-III) Tablet Cekamol 500 mg (Batch # T-5014)November 12, 2025
- Minutes of the 349th Meeting of the Registration BoardNovember 10, 2025
- Implementation of Pre-Import Clearance Mechanism under DRAP-PSW Gateway System for Import of Drugs (Raw Materials and Finished Products)November 6, 2025
- Decisions of the 104th Meeting of the Medical Device Board (MDB) held on 16-10-2025 (Part-II: Manual Applications)November 4, 2025
- 105. Recall Alert – Drug Products for Human Use Declared SubstandardOctober 30, 2025
- 104. Recall Alert – Veterinary Drug Products Declared Substandard.October 30, 2025
- Model List of National Essential Medicines (2025) – Notification Dated 20-10-2025October 28, 2025
- Product Specification of Mecobalamin / Methylcobalamin TabletOctober 28, 2025
- 103. Recall Alert – Drug Products Declared Substandard.October 28, 2025
- 102. Rapid Alert – Falsified / Spurious Veterinary Drug ProductsOctober 27, 2025
- 101. Recall Alert – Cream Kanadex-N (Batch # D7-22 & F7-27) – Substandard.October 24, 2025
- 100. Recall Alert – Veterinary Drug Products Declared Substandard.October 24, 2025
- Decisions of 103rd meeting of the Medical Device Board (MDB) held on 09-10-2025 (Part-II Manual Applications)October 23, 2025
- 99. Recall Alert (Class-II)- Drug Products Declared Substandard.October 22, 2025
