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REQUIREMENTS FOR APPLICATION OF CERTIFICATE OF FREE SALE (CFS) FOR EXPORT ONLY MEDICAL DEVICES NOVEMBER 2018
Hits: 10719
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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VOLUNTARY LISTING OF TECHNICAL PERSONNEL, TRAINING BODY (MeDTComp) OR COMPETENCY CERTIFICATION BODY UNDER MEDICAL DEVICE ACT 737
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LIST OF RENEW LICENSED ESTABLISHMENT
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SEARCH ENGINE FOR LICENSED ESTABLISHMENT
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PEMAKLUMAN PERTUKARAN ALAMAT LAMAN WEB, E-MEL & SISTEM MeDC@St PIHAK BERKUASA PERANTI PERUBATAN
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CIRCULAR LETTER NO.5 YEAR 2018 :- ADDITIONAL TRANSITION PERIOD FOR MEDICAL DEVICE LABBELING
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SUMMARY OF MEDICAL DEVICE-DRUG-COSMETIC INTERPHASE (MDDCI) PRODUCT CLASSIFICATION DECISION
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RECALL : VOLUNTARY RECALL OF DUREX REAL FEEL BATCH
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Home
Introduction
Background
Vision, Mission & Core Value
Functions
Organisation Chart
Code of Ethics and Conduct
Board of Directors
Top Management Team of MDA
Malaysian Leadership
Former CEO of MDA
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
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)
Annual Report
Customer Satisfaction Survey
Customer Satisfaction Survey Result
Customer Satisfaction Survey Report
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