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CIRCULAR LETTER NO. 4 YEAR 2018 (REVISION 1) : EXEMPTION FROM REGISTRATION REQUIREMENT FOR EXPORT ONLY MEDICAL DEVICE
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CIRCULAR LETTER NO.2 YEAR 2016(REVISION 1) : MEDICAL DEVICE PROCUREMENT FOR HEALTHCARE INSTITUTION
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CIRCULAR LETTER NO.4 YEAR 2014(REVISION 1) : MEDICAL DEVICE FOR IMPORT/EXPORT FROM / TO COUNTRIES WITHOUT DIPLOMATIC TIES WITH MALAYSIA
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PENGUMUMAN BERKAITAN PERMOHONAN PENDAFTARAN PERANTI PERUBATAN DAN PERLESENAN ESTABLISMEN DI BAWAH AKTA PERANTI PERUBATAN 2012 (AKTA 737) YANG MASIH TERTANGGUH SETELAH TAMAT TEMPOH PERALIHAN
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PELANTIKAN KETUA EKSEKUTIF PBPP YANG BARU
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LIST OF MEDICAL DEVICE REGISTRATION CERTIFICATES READY FOR COLLECTION FOR YEAR 2018
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RECALL: VOLUNTARY RECALL OF CLEAR & SIMPLE DIGITAL PREGNANCY TEST
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REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS) FOR EXPORT ONLY MEDICAL DEVICES NOVEMBER 2018
Hits: 9903
GUIDANCE DOCUMENT CHANGE NOTIFICATION FOR REGISTERED MEDICAL DEVICE, THIRD EDITION NOVEMBER 2018
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GUIDANCE DOCUMENT REQUIREMENTS FOR LABELLING OF MEDICAL DEVICES, THIRD EDITION NOVEMBER 2018
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Home
Introduction
Background
Vision, Mission & Core Value
Functions
Contact Us
Organisation Chart
Code of Ethics and Conduct
Board of Directors
Top Management
Division
Chief Executive's Office
Corporate Communication Unit
Legal Unit
Integrity Unit
Secretarial Unit
Pre-Market Control Division
Post Market & Enforcement Division
Policy & Strategic Planning Division
International and Industry Affairs Division
Management and Service Unit
FAQ
Single License Policy Implementation
Registration, Licensing & Enforcement
Labelling of Medical Devices
Technical Evaluation
Contact Us
Customer Complaint Form
Customer Satisfaction Survey
Staff Directory
Documents
Legislation
Circular Letter
Guidance Document
Guideline
Standard
General Directions
Strategic Plan
Slide Presentation
Infographic
Organizational Anti Corruption Plan (OACP) MDA 2022 - 2026
Buletin MDA
Press Release
Media Coverage (Newspaper Cutting)
Customer Satisfaction Survey Result
Annual Report
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