regulatory affairs professionals information, new medicinal product development guidelines, usa, uk

regulatory affairs professionals information
   
   
 Jobs
Clinical Project Manager 07 Dec 2017

 CMC Regulatory Affairs Associate – Biopharma 03 Jul 2008

 Regulatory Affairs Officer – Blue chip company 03 Jul 2008

 Regulatory Affairs Executive – Not just a Regulatory Executive Anymore 03 Jul 2008

 News on the Go
  Pocket PC Help
  i-mode Help
Help Pocket PC Web Site Help i-mode Web Site
You appear not to be registered. Please click here to find out what information packages we have on offer. If you have registered, please click here to log-in.



 Human Medicines
Australia - TGA: CMEC Minutes - October 2007 11 Jan 2008
Australia - TGA: Child-Resistant Packaging Stakeholder Consultation – January 2008 11 Jan 2008
Australia - TGA: CMEC Meeting Dates 2008 11 Jan 2008
USA - CBER: Cellular, Tissue and Gene Therapies Advisory Committee Meeting – February 2008 10 Jan 2008
USA - CBER: Fast Track Designation Request Performance Report – January 2008 10 Jan 2008
USA - CBER: Licensed Products and Establishments List – January 2008 10 Jan 2008

 Veterinary Medicines
EU - EMEA: Requests for Advice from CMD(v) to CVMP 09 Jan 2008
EU - EMEA: CHMP/CVMP QWP Work Programme 2008 16 Nov 2007
EU - EMEA: Experts Lists – Update October 2007 16 Nov 2007
EU - CVMP: "Sunset Clause" Q&A 16 Nov 2007
EU - CVMP: PSURs for Veterinary Medicinal Products – Draft Guideline 16 Nov 2007
EU - CVMP: Efficacy in Farmed Aquatic Species – Concept Paper 16 Nov 2007

 Medical Devices
Australia - TGA: MDSOs & CASOs Stakeholder Consultation – January 2008 11 Jan 2008
USA - CBER: Approved Biological Premarket Approval (PMA) Device Applications – January 2008 10 Jan 2008
USA - CBER: Cleared Biological 510(k) Device Applications – January 2008 10 Jan 2008
Australia - TGA: Medical Devices Transition – Update October 2007 19 Nov 2007
Global - GHTF: Presentations from GHTF 2007 16 Nov 2007
EU - EC: eHealth Standards and Interoperability 11 Oct 2007

 General Healthcare
Australia - TGA: MDSOs & CASOs Stakeholder Consultation – January 2008 11 Jan 2008
Denmark - DMA: Clear Objectives 2008 11 Jan 2008
Denmark - DMA: Advanced Therapy Medicinal Products Regulation 11 Jan 2008
USA - CBER: Fast Track Designation Request Performance Report – January 2008 10 Jan 2008
EU - EMEA: Road Map: 2008-2009 Implementation Phase 09 Jan 2008
EU - EMEA: ENCePP Meeting June 2007 – Report 09 Jan 2008


     
© 2000 - 2005 LORENZ Life Sciences Limited. reg123.com™ is a trademark of LORENZ Life Sciences Limited. Although care has been taken in the preparation of this web site the publisher, LORENZ Life Sciences Ltd or any of its content partners, cannot be held responsible for the accuracy of the information contained within the web site, nor for any consequence arising from such information. You are advised to seek additional advice when making decisions based on information you have obtained from this web site. Email the Webmaster with questions. This site was optimised for Internet Explorer 5.x or above. Home NS