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All Updates
- Rapid Alert – Unregistered / Illegal & Unsafe Sildenafil Tablets (PENAGRA, VEGA, COBRA) Being Sold IllegallySeptember 12, 2025
- Precautionary Recall of Inj. Cara-Fer (Iron Sucrose 100mg/5ml), Batch No. 24G001September 12, 2025
- RAPID ALERT – CRACKDOWN AGAINST UNLICENSED / UNAUTHORIZED MANUFACTURERSSeptember 10, 2025
- RAPID ALERT – SPURIOUS / FALSIFIED DECLARED BY PROVINCIAL LABORATORIES.September 10, 2025
- RECALL ALERT – FAMILA 28F TABLETS (Batch # K159, K196, K197, K198) DECLARED SUBSTANDARD.September 10, 2025
- RECALL ALERT – ANAROB INFUSION DECLARED SUBSTANDARD BY CENTRAL DRUGS LABORATORY, KARACHISeptember 9, 2025
- Invitation to bid for Supply of Chemicals, reagents, reference standard, glassware and kitsSeptember 5, 2025
- Decisions of the 94th & 96th Meeting of the Medical Device Board (MDB)September 2, 2025
- Submission of Required Details for Implementation of 2-D Barcode & Serialization by 1st September 2025August 29, 2025
- S.R.O. 1587(I)/2025 DRAP has adopted Pharmaceutical Inspection Co-operation Scheme (PIC/S) guidelinesAugust 26, 2025
- Directive for Submission of Antimicrobial Batch Production and Import Data in DRISAugust 26, 2025
- Minutes of 93rd meeting of Medical Devices BoardAugust 21, 2025
- 96th Meeting of Medical Devices Board will be held on 22nd August 2025August 20, 2025
- RAPID ALERT – CRACKDOWN AGAINST FALSIFIED / SPURIOUS DRUG PRODUCTSAugust 20, 2025
- RECALL ALERT – DRUG PRODUCTS DECLARED SUBSTANDARD BY CENTRAL DRUGS LABORATORY, KARACHI.August 18, 2025
- RAPID ALERT – CRACKDOWN AGAINST UNLICENSED/UNAUTHORIZED MANUFACTURERSAugust 11, 2025
- Recent Policy Updates and Procedural Guidelines for Drug Registration and ProcessingAugust 11, 2025
- VOLUNTARY RECALL ALERT – Amoxil Forte Suspension & Amoxil Suspension due to complaint of Induction Seal.August 5, 2025
- RECALL ALERT – BATCHES OF ‘TABLET FAMILA 28F’ DECLARED SUBSTANDARD BY CENTRAL DRUGS LABORATORY KARACHI.August 4, 2025
- Revised Regulatory Fee for Therapeutic GoodsAugust 4, 2025
- Decisions of 92nd Meeting of The Medical Device Board (MDB) held on 30-06-2025August 1, 2025
- Exemption for Import of Unregistered Drugs for use in Hospital and InstitutionsAugust 1, 2025
- Postponement of Interview for the Post of Assistant Director (RO-12), Drug Regulatory Authority of Pakistan (DRAP) at Lahore.July 30, 2025
- Recall Alert – MEDICAL DEVICES DECLARED SUBSTANDARD BY CENTRAL DRUGS LABORATORY KARACHI.July 29, 2025
- Interview call for the post of Assistant Directors at DRAP, Lahore OfficeJuly 29, 2025
- 94th Meeting of Medical Devices Board to be held on 31st July 2025July 28, 2025
- Minutes of the 348th Meeting of the Registration Board Held on 1st-2nd July, 2025July 24, 2025
- Notice for Documents Submission – Recruitment to the ten (10) posts of Deputy Director (Technical Cadre) (RO-13) – advertisement no. 01/2025July 24, 2025
- List of Establishment License under MDR 2017 (Local)July 23, 2025
- List of Establishment License under MDR 2017 (Import)July 23, 2025
- Requirement of Bio-equivalence Studies as part of Registration ApplicationJuly 23, 2025
- Inauguration of online system for the applications of Medical DevicesJuly 22, 2025
- Disposal of Applications of Biological ProductsJuly 22, 2025
- Health emergencies preparedness and risk management planJuly 21, 2025
- Guidance document for requirement of clinical trials or bio-similarity studies for registration of locally manufactured biological drugs for humansJuly 21, 2025
- Disposal of submitted applications of medical devicesJuly 19, 2025
- Introduction of online MDMC licensing and product registration portalJuly 19, 2025
- Pakistan Clinical Research Landscape Report 2025July 18, 2025
- DECISIONS OF 91ST MEETING OF MEDICAL DEVICE BOARD
HELD ON 17-06-2025July 11, 2025 - DECISIONS OF 90TH MEETING OF MEDICAL DEVICE BOARD
HELD ON 09-05-2025July 11, 2025 - DECISIONS OF 89TH MEETING OF MEDICAL DEVICE BOARD
HELD ON 24-04-2025July 11, 2025 - BIDDING DOCUMENT – APPOINTMENT OF TAX CONSULTANTJuly 10, 2025
- Tender for Conducting a National Pharmaceutical Pricing SurveyJuly 10, 2025
- Suspension of marketing authorisations of 17-Hydroxyprogesterone caproate (17- OHPC) due to its ineffectiveness in authorised usesJuly 9, 2025
- Risk of Meningioma with Medroxyprogesterone Acetate.July 9, 2025
- DRAP’s News Letter June 2025July 1, 2025
- Notification of draft amendments in the Drugs (Labelling and Packing) Rules 1986June 27, 2025
- Recall Alert: PRODUCTS DECLARED SUBSTANDARD BY PROVINCIAL DRUG TESTING LABORATORIESJune 27, 2025
- Internship program for future leaders in the Therapeutic Goods RegulationsJune 25, 2025
- Recall Alert: Recall of Substandard “Famobex Suspension” Batch No. 5330, Manufactured by M/s Cibex (Pvt.) Ltd, Karachi.June 24, 2025
