HighQ partners with SAFE-BioPharma

Wednesday, December 7, 2011 12:23 PM

London-based HighQ has formed a vendor partnership with the SAFE-BioPharma Association. Companies within the global pharmaceutical and biotechnology industry use the SAFE-BioPharma standard in FDA Title 21 CFR part 11 compliant processes for signing SOPs, quality and compliance documentation, research and development documentation, corporate compliance documents and more.

HighQ provides the life sciences industry with a unified space for secure document exchange and social collaboration across a global network of employees, researchers and partners – both internal and external to the company. HighQ Collaborate, a secure cloud-based platform, allows users to disseminate information to discovery teams, CROs, investigators and business development partners worldwide. Users will have the opportunity to securely exchange documents using their SAFE-BioPharma digital identities on the HighQ Collaborate platform, ensuring their credentials are available anytime and anywhere.

"By making use of collaborative tools such as wiki pages and blog posts alongside traditional office software (Word, Excel, PowerPoint, PDF etc.), sponsors, CROs and investigators can work more efficiently, eliminating the time consuming need to print out physical documents that require signatures during clinical trials. By partnering with the SAFE-BioPharma Association, HighQ will enable the life sciences industry to have an efficient, enforceable and regulatory-compliant document approval process, whilst facilitating secure document exchange and social collaboration throughout the organization," said Jacob Mathew, consultant – KM Practice, HighQ.

Share:          
CLINICAL TRIAL RESOURCES

Search:

NEWS ONLINE ARCHIVE

Browse by:

CWWeekly

October 20

Toronto Star, with FDA data, exposes weaknesses in Health Canada's clinical trial, inspection oversight

Crowdsourcing effort aims to fund updated online social media guide for sponsor interaction with patients

Already a subscriber?
Log in to your digital subscription.

Subscribe to CWWeekly.

The CenterWatch Monthly

September

Today's fastest, most economical sponsors
Standout sponsors reveal how they shorten regulatory, clinical cycle times

From the trenches: Sites' eye view of state of the industry
CW’s first site focus groups uncover frustration with 'progress,' but a passion for their mission

Already a subscriber?
Log in to your digital subscription.

Purchase the September issue.

Subscribe to
The CenterWatch Monthly.

The CenterWatch Monthly

August

Reality of costs and impact rain on Sunshine Act
Concerns mount over compliance burden on CROs, sponsors, unanticipated consequences for research

Cloud computing expanding into all areas of clinical trial conduct
Benefits outweigh the complexities, challenges of finding right vendors

Already a subscriber?
Log in to your digital subscription.

Purchase the August issue.

Subscribe to
The CenterWatch Monthly.

JobWatch centerwatch.com/jobwatch

Featured Jobs