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Latest Electronic trial master file Stories

2014-06-17 00:20:36

BARCELONA, Spain, June 17, 2014 /PRNewswire/ -- Research shows advanced eTMF technologies improve inspection readiness and compliance while reducing costs At this week's Drug Information Association's (DIA) 50th Annual Meeting, Veeva Systems released the results of the Veeva 2014 Paperless TMF Survey: An Industry Benchmark [http://www.veeva.com/tmf-survey-2014 ], the largest TMF survey to date. This in-depth study of more than 250...

2014-04-28 12:31:14

Company Integrates eTMF, CTMS and Investigator Portal to Bring Together Essential Clinical Trial Constituencies onto One Management System CONSHOHOCKEN, Pa., April 28, 2014 /PRNewswire/ -- NextDocs Corporation today announced that one of the world's leading pharmaceutical and biologics companies has leveraged the NextDocs clinical solution suite across more than 200 clinical trials to manage regulated content and compliance, and bring together clinical trial constituencies onto a...

2014-04-01 23:33:07

Forte Research, HL7, Kaiser Permanente, Mayo Clinic, Oracle, SureClinical, and Others Advance Interoperability Standard for Exchanging Clinical Trial Content in the Cloud. Rancho Cordova, CA (PRWEB) April 01, 2014 The pharmaceutical community, health care organizations, and software providers are coming together at the OASIS open standards consortium to define a machine-readable content classification standard for the interoperable exchange of clinical trial data via content management...

2013-12-30 23:01:18

Forward-thinking Biopharma and healthcare companies are increasingly looking to cloud-based computing solutions for digital document signing and completion. This approach helps in replacing labor-intensive paper document scanning and reducing document completion costs significantly, says SureClinical, a provider of collaborative cloud application solutions for Health Science that announced today the release of its new white paper, 'Estimating TMF Costs.' Rancho Cordova, California...

2013-11-01 23:25:58

New clinical trial eTMF Solution eliminates paper at the point of origination for productivity and cost savings. Rancho Cordova, California (PRWEB) October 31, 2013 To succeed in the increasingly regulated BioPharma clinical trial market, organizations need to ensure that clinical trial stakeholders can complete the growing mountain of regulatory documents efficiently, quickly, securely and cost effectively. Clinical trial study investigators, clinical research associates, clinical...

2013-09-30 23:18:27

Support growing for development of Electronic Trial Master File (eTMF) standard under OASIS Standards Development Group, according to non-profit CareLex. Silicon Valley, CA (PRWEB) September 30, 2013 CareLex, a nonprofit organization for BioInformatics research, today announced growing support for the development of an Electronic Trial Master File (eTMF) standard. The eTMF standard will modernize traditional paper-based clinical trial data through a new data exchange standard for...

2013-09-04 23:22:05

BioPharma Group to Convene Electronic Trial Master File (eTMF) Standard Technical Committee at OASIS Silicon Valley, California (PRWEB) September 04, 2013 CareLex, a non-profit organization for BioInformatics research, today announced plans to develop an Electronic Trial Master File (eTMF) standard that will modernize traditional paper-based clinical trial data by enabling the use of interoperable information systems. The work, which will build on the recently published eTMF Reference...

2013-08-01 23:25:43

First eTMF Cloud Software Solution To Completely Address FDA 21 CFR Part 11 Regulations Rancho Cordova, CA (PRWEB) August 01, 2013 SureClinical, a provider of cloud-based content management application software and services for health sciences, announced today that it has successfully completed an FDA 21 CFR Part 11 compliance audit of its SureTrial® eTMF clinical trials content management application. More information is available at http://www.SureTrial.com. Conducted through a...


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