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Medical Devices
Web Assisted Notification of Devices (WAND)

Archived Information

This may be useful for reference but some information may no longer be relevant.

1. July 2010 Presentation made at the "Healthcare Materials Management and Medical Technology Association of NZ 6th Combined Annual Conference 26th - 28th July 2010

• WAND Regulatory Issues 2010  (Microsoft Powerpoint document 163KB)

2. July 2008 Presentations made at the "Healthcare Materials Management and Medical Industry Association of NZ 4th Combined Annual Conference 28th - 30th July 2008

• MIANZ presentation-When Things Aren't Right (Adobe Acrobat (pdf) document 420KB)
• WAND Regulatory Issues 08 (Microsoft Powerpoint document 163KB)

2. June 2007 WAND workshop presentation (Microsoft Powerpoint 455 KB)
3. November 2005 Medsafe, MIANZ and the TGA Roadshow

• General Session

• General Session - WAND Update (Adobe Acrobat document 289KB)
• Elements of the Regulatory Framework for Medical Devices (Adobe Acrobat document 237KB

• Manufacturers Session)
  • Introduction and WAND information (Adobe Acrobat document 24KB)
  • The Roadmap for Manufacturers (Adobe Acrobat document 518KB)

• IVD Session

1. Introduction (Adobe Acrobat document 40KB)
2. The Proposed Regulatory Framework for IVDs (Adobe Acrobat document 185KB)

4. October 2005 Presentations given at the Healthcare Materials Management & Medical Industry Association of New Zealand 1st Combined Annual Conference, at the Town Hall, Wellington Convention Centre:
    
   • Recalls & Alerts . Who is responsible? (Microsoft Powerpoint presentation 339KB)
   • Wand Update. Kits & Packs. Regulatory Impact for Importers, DHBs & Manufacturers. Are DHBs manufacturers? (Microsoft Powerpoint presentation 184KB)
5. December 2004 Presentations from the In-Vitro Diagnostics Seminar
   (Please note these are Microsoft powerpoint files.  You will need either Microsoft Powerpoint or Microsoft Powerpoint Viewer to view these files.  Please click here to download the viewer.)

• The Trans Tasman Therapeutic Products Scheme (Microsoft Powerpoint presentation 136KB)
• Introduction - Proposed Requirements for In-vitro Diagnostic Devices (Microsoft Powerpoint presentation 694KB)
• The Global Position on IVD Regulation (Microsoft Powerpoint presentation 218KB)
• Essential Principles and Standards (Microsoft Powerpoint presentation 268KB)
• Classifying your IVD (Microsoft Powerpoint presentation 163KB)
• Proposed Regulatory Framework for IVDs - Conformity Assessment Procedures (Microsoft Powerpoint presentation 172KB)
• The Application Process (Microsoft Powerpoint presentation 143KB)
• Transition Arrangments (Microsoft Powerpoint presentation 220KB)

6. November 2003 Letter sent to device suppliers in Nov 2003