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TRAINING FOR RE-REGISTRATION FOR CAB AUDITORS AND TECHNICAL PERSONNEL UNDER ACT 737 (COMPLIANCE TO THE CONFORMITY ASSESSMENT BODY REGISTRATION REQUIREMENTS)
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TRAINING BY THE MEDICAL DEVICE AUTHORITY ON GOOD DISTRIBUTION PRACTICE FOR MEDICAL DEVICE (GDPMD) FOR LEAD AUDITOR
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PEMBATALAN SIJIL PERANTI PERUBATAN
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SECOND EDITION GUIDANCE DOCUMENT MDA/GD/0027: LICENSING FOR ESTABLISHMENTS
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ONLINE TRAINING ON ISO 14155:2020 CLINICAL INVESTIGATION OF MEDICAL DEVICES FOR HUMAN SUBJECTS – GOOD CLINICAL PRACTICE
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GUIDELINE RE-REGISTRATION OF REGISTERED MEDICAL DEVICE
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MEDICAL DEVICE AUTHORITY INDUSTRY DIALOGUE 2022
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SEMINAR KAWALAN PENGIKLANAN ANJURAN PIHAK BERKUASA PERANTI PERUBATAN (MDA) “BOLEH PERCAYA KE IKLAN INI?” OKTOBER 13, 2022 PENGUMUMAN PERTAMA
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Home
Introduction
Background
Vision, Mission & Core Value
Objectives
Contact Us
Organisation Chart
Code of Ethics and Conduct
Board of Directors
Division
Chief Executive's Office
Corporate Communication Unit
Legal Unit
Integrity Unit
Pre-Market Division & Post-Market and Enforcement Division
Policy, International Affairs and Industry Facilitation (DASAR)
Management and Service Unit
FAQ
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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