STAMFORD, CT— April 13, 2015— ArisGlobal, a leading provider of solutions to the life sciences industry, has today announced the availability of agFileMaster; a Cloud-based electronic trial master file (eTMF) solution that serves as a centralized, global repository for managing all clinical trial-related documents in accordance with GCP standards and applicable regulatory requirements.
agFileMaster can be deployed either as a stand-alone solution or unified as part of ArisGlobal’s Clinical Trial Management System (CTMS). Life science organizations can overcome the complex burden of collecting, organizing and tracking the vast amount of essential trial documents from a multitude of disparate content management repositories with a single solution that provides real-time, controlled access to essential trial documentation.
Fully validated, agFileMaster supports the DIA TMF Reference model and is 21 CFR Part 11 compliant, helping to ensure the TMF file structure and organization is ready for audit and inspection. Full, context-sensitive document management capabilities and integrated workflows support and streamline key business processes to speed up site set-up and initiation and ensure patient recruitment can start as early as possible.
“Many of today’s current eTMF solutions are falling short of what is needed,” said Simon Sparkes, Executive Vice President, Product Strategy at ArisGlobal. “We need to be able to more than just organize documents. A modern eTMF needs to be able to identify documents required for each country and entity, identifing missing documents while allowing online exchange with sites. Ultimately, the aim of any eTMF is to support a submission/approval process. Our eTMF fully supports the tracking of all documents required for approval as well as tracking the submission itself. Of course an eTMF becomes truly effective when integrated with a CTMS. agFileMaster goes beyond the limitations of traditional integration of incompatible vendor solutions and is part of our fully unified clinical operations platform including agClinical CTMS ”
Like all of ArisGlobal’s clinical development solutions, agFileMaster is available for rapid, Cloud-based implementation via ArisGlobal's highly proven, regulated Cloud platform. agFileMaster can be deployed either as a stand-alone solution or unified as part of our CTMS offering.
Connect with ArisGlobal
• View the on-demand webinar, “Maximizing eTMF and eClinical Solutions for Improved Metrics and IRB Submissions”.
• Read the white paper on “Understanding True eTMF Requirements”.
• Join the discussion on our blog, Totally Clinical, where you can join the conversation on a wide range of clinical development topics, including this three-part series on the benefits of a unified solution
• Find us on LinkedIn
About ArisGlobal
For over 25 years ArisGlobal (www.arisglobal.com) has been a leading provider of integrated software solutions for pharmacovigilance and safety, regulatory affairs, clinical research and quality & compliance for medical inquiries. Solutions are available on premise or on a regulated Cloud platform. Life science companies using ArisGlobal’s solutions can better build and maintain the trust they need with their customers, medical practitioners and regulatory bodies around the world.
Contacts
Kathy Capper
ArisGlobal
+ 44 (0) 1908 340 838
kcapper@arisglobal.com
Help employers find you! Check out all the jobs and post your resume.
agFileMaster can be deployed either as a stand-alone solution or unified as part of ArisGlobal’s Clinical Trial Management System (CTMS). Life science organizations can overcome the complex burden of collecting, organizing and tracking the vast amount of essential trial documents from a multitude of disparate content management repositories with a single solution that provides real-time, controlled access to essential trial documentation.
Fully validated, agFileMaster supports the DIA TMF Reference model and is 21 CFR Part 11 compliant, helping to ensure the TMF file structure and organization is ready for audit and inspection. Full, context-sensitive document management capabilities and integrated workflows support and streamline key business processes to speed up site set-up and initiation and ensure patient recruitment can start as early as possible.
“Many of today’s current eTMF solutions are falling short of what is needed,” said Simon Sparkes, Executive Vice President, Product Strategy at ArisGlobal. “We need to be able to more than just organize documents. A modern eTMF needs to be able to identify documents required for each country and entity, identifing missing documents while allowing online exchange with sites. Ultimately, the aim of any eTMF is to support a submission/approval process. Our eTMF fully supports the tracking of all documents required for approval as well as tracking the submission itself. Of course an eTMF becomes truly effective when integrated with a CTMS. agFileMaster goes beyond the limitations of traditional integration of incompatible vendor solutions and is part of our fully unified clinical operations platform including agClinical CTMS ”
Like all of ArisGlobal’s clinical development solutions, agFileMaster is available for rapid, Cloud-based implementation via ArisGlobal's highly proven, regulated Cloud platform. agFileMaster can be deployed either as a stand-alone solution or unified as part of our CTMS offering.
Connect with ArisGlobal
• View the on-demand webinar, “Maximizing eTMF and eClinical Solutions for Improved Metrics and IRB Submissions”.
• Read the white paper on “Understanding True eTMF Requirements”.
• Join the discussion on our blog, Totally Clinical, where you can join the conversation on a wide range of clinical development topics, including this three-part series on the benefits of a unified solution
• Find us on LinkedIn
About ArisGlobal
For over 25 years ArisGlobal (www.arisglobal.com) has been a leading provider of integrated software solutions for pharmacovigilance and safety, regulatory affairs, clinical research and quality & compliance for medical inquiries. Solutions are available on premise or on a regulated Cloud platform. Life science companies using ArisGlobal’s solutions can better build and maintain the trust they need with their customers, medical practitioners and regulatory bodies around the world.
Contacts
Kathy Capper
ArisGlobal
+ 44 (0) 1908 340 838
kcapper@arisglobal.com
Help employers find you! Check out all the jobs and post your resume.
