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ISO 13485:2016 QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES
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POSSIBLE WAYS TO REGISTER IVD ANALYZER
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JAWATAN KEKOSONGAN DI MEDICAL DEVICE AUTHORITY (MDA) KEMENTERIAN KESIHATAN MALAYSIA
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PENGUMUMAN PENTING PERMOHONAN IKLAN PERANTI PERUBATAN 2023
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REGULATORY TRAINING - POST MARKET REQUIREMENTS
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Last chance to join TRAINING BY THE MEDICAL DEVICE AUTHORITY 0N INTRODUCTION TO BIOMEDICAL TECHNICAL PERSONNEL ON 31st OCTOBER 2023
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PENGUMUMAN : PELAKSANAAN PENGGUNAAN SIJIL PENDAFTARAN PERANTI PERUBATAN ELEKTRONIK SEPENUHNYA BERMULA 1 NOVEMBER 2023
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MDA TO CEASE THE ISSUANCE OF CERTIFICATE OF FREE SALE (CFS) FOR EXPORT ONLY MEDICAL DEVICE
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MEDICAL DEVICE RECALL: BIO-AQUACEL EYE SAFE
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INTRODUCTION TO REGULATORY REQUIREMENTS FOR BIOMEDICAL TECHNICAL PERSONNEL (BTP) REGISTRATION IS NOW CLOSED!
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Home
Pengenalan
Latar Belakang
Visi, Misi & Nilai Teras
Objektif
Hubungi Kami
Carta Organisasi
Code of Ethics and Conduct
Board of Directors
Top Management
Bahagian
Pejabat Ketua Eksekutif
Unit Komunikasi Korporat
Unit Undang-undang
Unit Integriti
Secretarial Unit
Bahagian Pendaftaran, Pelesenan Dan Penguatkuasaan
Post Market & Enforcement Division
Policy & Strategic Planning Division
International and Industry Affairs Division
Unit Pengurusan Dan Perkhidmatan
Soalan Lazim
Single License Policy Implementation
Pendaftaran, Pelesenan & Penguatkuasaan
Labelling of Medical Devices
Technical Evaluation
Hubungi
Borang Aduan Pelanggan
Kajian Kepuasan Pelanggan
Direktori Kakitangan
Dokumen
Perundangan
Surat Pekeliling
Dokumen Panduan
Garis panduan
Standard
General Directions
Strategic Plan
Persembahan Slide
Infographic
Organizational Anti Corruption Plan (OACP) MDA 2022 - 2026
Buletin MDA
Press Release
Media Coverage (Newspaper Cutting)
Customer Satisfaction Survey Result
Laporan Tahunan
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