Skip to content
All Updates
- 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
- 98-Rapid Alert- Falsified / Unregistered Aphrodisiac Drug ProductOctober 22, 2025
- 97- RECALL ALERT – VETERINARY DRUG PRODUCT DECLARED MISBRANDEDOctober 22, 2025
- 96. RAPID ALERT – FALSIFIED / SPURIOUS – CIALIS®October 20, 2025
- Decision of Enlistment Evaluation Committee (EEC) regarding revocation of provisional firm enlistment (Form-6) of M/s Nutris Lab, Lahore due to shifting of facility to new premisesOctober 17, 2025
- Decisions of 100th meeting of the Medical Device Board (MDB) held on 18-09-2025 (Part-I MDL&R Portal Agenda)October 17, 2025
- Expression of interest (EOI) for hiring of storage warehouse / shed through EPADS for storage of official record – an open framework agreementOctober 17, 2025
- Invitation to bid: provision of housekeeping, janitorial & support staff at DRAP officesOctober 17, 2025
- Mandatory Sourcing Requirements for Active Pharmaceutical Ingredients (APIs)/Drug Substances (DS) Imported for Product Development, Stability Studies and Commercial ManufacturingOctober 17, 2025
- Minutes of 351st Meeting of Registration Board (23rd – 24th September, 2025)October 17, 2025
- Advisory to Therapeutic Goods Manufacturers: Measures to Prevent DEG/EG Contamination in Oral Liquid PreparationsOctober 16, 2025
- 95. Recall Alert – Veterinary Drug Product declared Substandard.October 16, 2025
- 94. Recall Alert (Class-II) – Substandard Drug Products.October 16, 2025
- 93. Recall Alert- Syrup Synadin 60ml (Batch # L24K110) -SubstandardOctober 16, 2025
- RAPID ALERT – SPURIOUS / FALSIFIED (TABLET FEMARA 2.5 mg)October 16, 2025
- RAPID ALERT – SPURIOUS/FALSIFIED (TABLET MYTEKA 10 mg)October 16, 2025
- Recall Alert – Tablet Cloferd 50 mg (Batch # 6926) declared Substandard.October 15, 2025
- Recall Alert – Adulterated Tablet Virtec 10 mg (Batch # FK-24-007)October 15, 2025
- RAPID ALERT – CRACKDOWN AGAINST UNLICENSED / UNAUTHORIZED MANUFACTURERSOctober 14, 2025
- RAPID ALERT – SPURIOUS DETECTED – Injection OXYZON 5% (Veterinary)October 13, 2025
- Recall Alert – Drug Products declared substandardOctober 9, 2025
- RAPID ALERT – FALSIFIED / UNAUTHORIZED MANUFACTUREROctober 9, 2025
- Recall Alert – Veterinary Drug Products (Substandard)October 9, 2025
- RAPID ALERT: UNREGISTERED & SUBSTANDARD — LEVITRA 20 mg TABLET (Batch BXNZ2488)October 8, 2025
- Guidelines for Referring the Cases for Prosecution under the DRAP Act, 2012 and the Drugs Act, 1976October 6, 2025
- Minutes of 350th Meeting of the Registration BoardOctober 6, 2025
- Minutes of M-99 of the Medical Devices BoardOctober 6, 2025
- Recall Alert – Orange Auto disable Syringes 5mL (Batch # S5102402), DECLARED SUBSTANDARD BY CENTRAL DRUGS LABORATORY KARACHI.September 30, 2025
- RAPID ALERT – FALSIFIED / SPURIOUS DRUG PRODUCT IN THE MARKET.September 26, 2025
- RECALL ALERT -TABLET AMLOshine (all strengths & batches) – Sunshine PharmaceuticalsSeptember 26, 2025
- RECALL ALERT – DRUG PRODUCTS (CLASS – I).September 25, 2025
- RECALL ALERT – TABLET ASCARD-75 (Batch # AR046L)September 25, 2025
- Recall Alert – Class II (Tablet Ascard-75) Batch # AR021LSeptember 23, 2025
- RECALL ALERT – Class I – Substandard drug ProductsSeptember 23, 2025
- Mandatory submission of lot release applications for biological products through the online lot release portalSeptember 23, 2025
- RECALL ALERT – PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIESSeptember 19, 2025
- RAPID ALERT – CRACKDOWN AGAINST FALSIFIED / SPURIOUS PRODUCTSSeptember 19, 2025
- VETERINARY DRUG PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIES.September 18, 2025
- RECALL ALERT – DRUG PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIES.September 18, 2025
