The TMF & Inspection Readiness Forum is returning to Amsterdam for its 4th iteration this September 24th-27th !
Montrium invites you to join this year's interactive sessions that discuss new innovative strategies and address key issues in eTMF integration and control, debate over best practice, CRO v Sponsor TMF management and scanning verifications.
WHY VISIT?
- Prepare for inspections and audits through our exclusive pre-conference training day
- Learn how to optimise the use of eTMF platforms to increase efficiency in documentation management
- Debate CRO vs Sponsor TMF management and the exchange of responsibilities with peers and experts
- Understand the different expectations of global inspectors and how to be inspection ready 100% of the time
- Establish best practice in preparing documentation for inspection and integrating eTMF platforms
Save 10% extra off the ticket price with your Montrium discount!
Montrium!10
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FEATURED SPEAKERS
Evi De Ruymaeker, Head of TMF Operations, Study Delivery Management, GSK
Francisca Diala, Clinical Research specialist (Clinical Documentation), AbbVie
Jamie Toth
Head of TMF Operations,
Daiichi Sankyo
Paul Fenton, Steering Committee Member, TMF Reference Model and Sub-group Cochair, eTMF-EMS
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FEATURED INDUSTRY RESOURCES
Many sponsors and CROs have now migrated from traditional paper Trial Master Files onto eTMF systems; this brings about several issues in terms of ease of exchange when moving TMF content between different eTMF vendor systems.
In this exclusive interview we discussed:
- Which key benefits will be gained from a common standard for the exchange of TMF documents
- How the standardised exchange of TMF using the new specification will affect the relationship between sponsors, CROs and the vendors
- How the standard is likely to shape the future of eTMF system exchange
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ABOUT Montrium
Montrium is a global technology leader in Document & Quality Management software for the Life Sciences industry, working for over 10 years to improve the way organizations use technology. We focus on leveraging our deep understanding of GxP processes and technologies to provide cost-effective solutions for pharmaceutical, biotechnology, contract research, manufacturing and medical device industries. Montrium’s Electronic Trial Master File solution, eTMF Connect, centralizes and standardizes your clinical records, enabling both sponsors and CRO’s to contribute and access important clinical content in real time. From collaborating and managing clinical documentation to reporting on TMF completeness and driving better clinical decisions, eTMF Connect significantly increases end-to-end visibility and oversight throughout your clinical programs.
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