DGE’S 2nd Electronic Trial Master File Forum To Showcase Leading Industry Faculty For Tips On TMF Technology For Successful Clinical Research

Online Livestreaming Event Date: August 16-17, 2021 Clinical researchers, medical managers, pharma companies, and life science professionals are invited to attend the 2nd Electronic Trial Master File (“eTMF”) Forum on August 16-17th, 2021. This 2-day event will offer a leading stage to learn the skills of integrated TMF technology for successful clinical research. Attendees will understand the intricacies of identifying the challenges and risks posed during clinical research. They will learn to identify how to protect the data gathered during the research trials, meeting regulatory requirements, preparing for audits, getting ready for inspections, and lucrative techniques for monitoring and filing correspondence. The event is powered by the Scaritt Group, Inc. and the TMF Professionals. The 2nd eTMF Forum is hosted by Dynamic Global Events (“DGE”), a Life Science Leader in organizing B2B Events. The Global Event Company caters to the dynamic informational and networking needs of the Pharmaceutical, Biotechnology, Healthcare, Medical Devices, and allied industries. The 2nd Electronic Trial Master File Forum is an online live streaming event that will witness the leading industry stalwarts from around the globe sharing their opinion, views and perspective about seamlessly conducting clinical trial research. Some important elements of the event’s agenda include:

• Stay ahead in competition through advanced inspection readiness solutions
• Data privacy risks and challenges for intellectual property
• Improving collaboration techniques between CROs and sites
• Ensure a secure quality monitoring and quality-control procedure
• Communicate the expectation of the completion time of a completeness review
• Communicate the work instructions among the sponsors and third parties and align with SOPs

The 2nd Electronic Trial Master File Forum is of special interest to Solution Providers, Paper and Electronic Archiving systems, Clinical Research Organizations, Data Records Managers, and eTMF Service Providers, who will get an overview of pre and post-inspection readiness and recognize the importance of timing and readability. They will further learn the use of technology for maximum integration and explore completeness review from a resourcing and staffing perspective. Speakers at the event will discuss how an inspection ready TMF requires a comprehensive approach, accounting for variables, and sound evaluation of parameters that could go wrong. Refining collaborative processes with CROs and understanding their requirements and motivations are some of the key lessons that will be discussed at the Forum. To know more about the event, please visit https://ibn.fm/9Qfkt