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KENYATAAN MEDIA PERLUASAN PENJUALAN KIT UJIAN KENDIRI COVID-19
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TRAININGS ON ISO 13485:2016 QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES - 10 & 11 NOVEMBER 2021
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COMPULSORY COMPETENCY MODULE: INTRODUCTION TO REGULATORY REQUIREMENTS FOR BIOMEDICAL TECHNICAL PERSONNEL (BTP)
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TRAININGS FOR CONFORMITY ASSESSMENT BODY (TRAININGS SANCTIONED BY THE MEDICAL DEVICE AUTHORITY)
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MEDICAL DEVICE WEBINAR 2021 - POLICY UPDATES AND NEW MEDICAL DEVICE REGULATIONS UNDER ACT 737 : ADVERTISEMENT , POST MARKET REQUIREMENTS AND MEDICAL DEVICE RE- REGISTRATION
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REQUIREMENTS FOR REGISTRATION MEDICAL GAS SYSTEM - AWARENESS PROGRAM
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COMPULSORY COMPETENCY MODULE: INTRODUCTION TO REGULATORY REQUIREMENTS FOR BIOMEDICAL TECHNICAL PERSONNEL (BTP) SEPTEMBER 2021
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PEMBATALAN SURAT PEKELILING PIHAK BERKUASA PERANTI PERUBATAN (PBPP) BIL 1/2014
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PENGIMPORTAN DAN PENGEDARAN KIT UJIAN KENDIRI COVID-19 MELALUI KELULUSAN BERSYARAT (CONDITIONAL APPROVAL)
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Home
Introduction
Background
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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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