Whats New
Guidance Documents (IVD)
A. Guidance Documents on In Vitro Diagnostic (IVD) Medical Device
The following are the draft Guidance Documents on IVD medical device prepared by Medical Device Control Division for public comment:
1. Essential Principles of Safety and Performance for IVD Medical Devices
2. IVD Medical Device Classification System
3. Conformity Assessment for IVD Medical Devices
4. Common Submission Dossier Template (CSDT) of IVD Medical Device
You are welcome to give comment and feedback on the draft documents. Please list all your comment in the Comment Form and submit it to mdb@mdb.gov.my before 31 January 2012.
Resource:
i. Global Harmonization Task Force (GHTF)
ii. ASEAN Consultative Committee for Standards and Quality - Product Working Group on Medical Device( ACCSQ – MDPWG)
B. Guidance Document on Product Grouping
The following is the draft Guidance Documents Product Grouping prepared by Medical Device Control Division for public comment:
1. Product Grouping
You are welcome to give comment and feedback on the draft document. Please list all your comment in the Comment Form and submit it to mdb@mdb.gov.my before 31 January 2012.
Guidance Documents
Guidance Documents
The following are the list of draft guidance documents and the presentation on the Proposed Medical Device Registration System prepared by this division.
You may download these documents for your information on our proposed Medical Device Regulation.
These draft guidance documents and the presentation can be downloaded from this page.
List of Draft Guidance Documents
- Guidance on The Definition of Medical Device
- Guidance on The Classification of Medical Device
- Guidance on The Essential Principles of Safety and Performance of Medical Device
- Guidance on The Common Submission Dossier Template For Medical Device
- Regulatory Requirement on Good Distribution Practice
- The Proposed Medical Device Registration System
Resource:
i) GHTF
ii) HAS
iii) EU
