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PUBLIC COMMENT DRAFT MEDICAL DEVICE GUIDANCE DOCUMENT RULES OF CLASSIFICATION FOR GENERAL MEDICAL DEVICES
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SEMINAR BY THE MEDICAL DEVICE AUTHORITY 2022 REGULATORY UPDATES AND FACILITATION TOWARDS ADDRESSING THE CHALLENGES OF THE COVID-19 PANDEMIC MARCH 31, 2022
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FIRST EDITION GUIDANCE DOCUMENT MDA/GD/0060: REFURBISHED MEDICAL DEVICE-REQUIREMENTS
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KENYATAAN MEDIA
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KEPERLUAN PENDAFTARAN PERANTI PERUBATAN DAN LESEN ESTABLISMEN DI BAWAH SEKSYEN 5 DAN 15 AKTA PERANTI PERUBATAN 2012 (AKTA 737) BAGI MANA-MANA INDIVIDU, SYARIKAT ATAU FASILITI KESIHATAN YANG MENJALANKAN AKTIVITI RANTAIAN PEMBEKALAN PERANTI PERUBATAN
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Home
Introduction
Background
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Board of Directors
Top Management
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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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