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CAB_2024

Pengujian
22 & 23 November 2022 - Training For Re-Registration For CAB Auditors And Technical Personnel Under Act 737 (Compliance To The Conformity Assessment Body Registration Requirements)
29 & 30 June 2022 - Training for Renewal of Registration for Cab Auditors and Technical Persons (For the Purpose of Medical Device Registration Under the Act 737)
14 & 15 February 2022 - Training On Conformity Assessment Procedures On Technical Documentation & Verification (For The Purpose Of Medical Device Registration Under The Act 737)
16 February 2022 - Training On Conformity Assessment Body Registration Under The Act 737 (Medical Device Act & Regulations 2012)
17 February 2022 - Training On Conformity Assessment Procedures On QMS & PMSS (For The Purpose Of Establishment Licensing Under The Act 737)
25 May 2022 - Training On Conformity Assessment Body Registration Under The Act 737 (Medical Device Act & Regulations 2012)
26 May 2022 - Training On Conformity Assessment Procedures On QMS & PMSS (For The Purpose Of Establishment Licensing Under The Act 737)
15 & 16 August 2022 - Training On Conformity Assessment Procedures On Technical Documentation & Verification (For The Purpose Of Medical Device Registration Under The Act 737)
23 & 24 May 2022 - Training On Conformity Assessment Procedures On Technical Documentation & Verification (For The Purpose Of Medical Device Registration Under The Act 737)
18 August 2022 - Training On Conformity Assessment Procedures On QMS & PMSS (For The Purpose Of Establishment Licensing Under The Act 737)
14 & 15 November 2022 - Training On Conformity Assessment Procedures On Technical Documentation & Verification (For The Purpose Of Medical Device Registration Under The Act 737)
16 November 2022 - Training On Conformity Assessment Body Registration Under The Act 737 (Medical Device Act & Regulations 2012)
17 November 2022 - Training On Conformity Assessment Procedures On QMS & PMSS (For The Purpose Of Establishment Licensing Under The Act 737)
17 August 2022 - Training On Conformity Assessment Body Registration Under The Act 737 (Medical Device Act & Regulations 2012)
15 & 16 DECEMBER 2021 - GOOD DISTRIBUTION PRACTICE FOR MEDICAL DEVICES (GDPMD) (ONLINE TRAINING)
10 & 11 NOVEMBER 2021 - ISO 13485:2016 QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES (ONLINE TRAINING)
29 October 2021 - Training On Remote Audit (For The Purpose Remote Audit)
28 October 2021 - Training On Conformity Assessment Procedures On QMS & PMSS (For The Purpose Of Establishment Licensing Under The Act 737)
27 October 2021 - Training On Conformity Assessment Body Registration Under The Act 737 (Medical Device Act & Regulations 2012)
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Medical Device Authority (MDA), Ministry of Health Malaysia, Level 6, Prima 9, Prima Avenue II, Block 3547, Persiaran APEC, 63000 Cyberjaya, Selangor, MALAYSIA

Phone: +603 - 8230 0300

E-mail: mdb@mda.gov.my

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