News and Events

Clarmon is sponsoring the following events:

• Clinical IT Systems Europe 2008 (London, 23-25 April 2008)
• Software Validation: How to Reduce Time and Costs while Managing Risk (Singapore, 5 May 2008)
• Pharma IT Systems Asia-Pacific 2008 (Melbourne, 7-9 May 2008)
• Pharma IT Systems Asia-Pacific 2008 (Sydney 12-14 May 2008)
• Pharma IT Systems Ireland 2008 (Cork, IRELAND, 9 – 13 June 2008)
• Pharma IT Systems Europe 2008 (London, 22 – 26 September 2008)
• Pharma Software Validation Europe 2008 ( London, 27 & 28 November 2008)
  
  

Press Releases

London,
February 13, 2008
Clarmon and partner Csols will showcase QAvalid™ at Pitcon 2008 - Booth #5162

Clarmon Corporation will be presenting QAvalid™, its advanced compliance management application at PITTCON 2008 at the Ernest N. Morial Convention Center in New Orleans, Louisiana, March 1-7.

To read the entire press release, click here. (viewing requires Adobe Reader)


London
January, 7, 2008
Dr Siegfried Schmitt has joined Clarmon’s advisory board.

Clarmon Corporation is proud to welcome Dr. Siegfried Schmitt as the newest member on the advisory board. His experience in computerized systems, pharmaceuticals and medical devices will be leveraged to increase the efficiency of Clarmon’s compliance management solutions.

To read the entire press release, click here. (viewing requires Adobe Reader)

London & Magdeburg
August, 12, 2007
QAvalid™ will help Germany’s Statconsult better manage data throughout their projects.

Clarmon Corporation announced that it will provide its QAvalid™ solution to German company Statconsult.
Statconsult has more than 15 years of experience in Biometrics and Data Management and will be using QAvalid™ mainly to improve Quality Assurance Activities.

To read the entire press release, click here. (viewing requires Adobe Reader)


Newark, Delaware
June 15th, 2007
Clarmon joins forces with Csols

Clarmon Corporation announces signing an agreement with laboratory informatics company, Csols. The agreement will set the base for a valuable partnership between the two companies. Csols experience in the Pharmaceutical and Biotechnology industries will combine with Clarmon’s premier product, QAvalid™ to deliver advanced solutions for validating laboratory systems.

To read the entire press release, click here. (viewing requires Adobe Reader)

London
April 30th, 2007
M+W Zander to use QAvalid™

Clarmon Corporation. announced today that it has signed an agreement to provide its unique compliance management application QAvalid™ application to M+W Zander.
M+W Zander, a globally active technology enterprise with an 8,000-strong workforce at more than 40 company sites worldwide will use QAvalid™ application developed by Clarmon to streamline its Quality Assurance process.

To read the entire press release, click here. (viewing requires Adobe Reader)


London
March 26th, 2007
QAvalid™ selected by DynaLink Pharma

Clarmon Inc. today announced an agreement with Singapore based DynaLink Pharma that will involve deployment of its QAvalid™ compliance management solution.
DynaLink Pharma will use QAvalid™, the innovative compliance management application developed by Clarmon Inc. to handle regulatory issues more efficiently.

To read the entire press release, click here. (viewing requires Adobe Reader)


London
November 29th, 2006
Singapore based Link Biotechnologies will rely on QAvalid™ for its compliance management.

LYNK BIOTECHNOLOGIES, a rapidly growing Singaporean biopharmaceutical company, has chosen Clarmon’s QAvalid™ as an integrated and cost-effective solution compliance management application to deal with the company’s GMP quality assurance challenges.

To read the entire press release, click here. (viewing requires Adobe Reader)


London
August, 27, 2006
Gulf Pharmaceuticals, Julphar - the largest generic drug manufacturer in the UAE chooses QAvalid™ to facilitate FDA compliance.

Clarmon Corporation announced today the completion of an agreement with Gulf Pharmaceutical Industries (Julphar). Clarmon will deliver QAvalid™, an innovative and fully integrated compliance management solution to help Julphar manage its FDA / GMP compliance processes in an easy and cost-effective manner.

To read the entire press release, click here. (viewing requires Adobe Reader)