VeraClinical Trials & the TMF 101Blog 3: Paper vs Electronic, why it is more than a DMSDec 7, 2022Dec 7, 2022
VeraUS FDA Provides Reminders for Upcoming eCTD Validation ChangesThe DIA Regulatory Submissions, Information, and Document Management (RSIDM) Forum, held online and in person from February 14 to 16, was…Jul 28, 2022Jul 28, 2022
VeraHow Quality Review and Heatmaps Can Reduce Remediation Time, Cost, and Effort for an Acquired Trial…Posted by Karen Roy and Sarah TuckerJul 27, 2022Jul 27, 2022
VeraWhy Is the Trial Master File Critical in M&A activities?Adapted from a Phlexglobal Ask An Expert seminar, “How to Ensure TMF Inspection Readiness & Compliance for a Recently Acquired Product,”…Jul 26, 2022Jul 26, 2022
VeraDecision Criteria for the Next Generation of Regulatory Information Management (RIM) SystemsPosted by Jim Nichols and Aaron GrantJul 22, 2022Jul 22, 2022
VeraSponsors Gear Up For a Smoother Process With CTIS but Must First Overcome Key HurdlesPosted by Milena Shuytsova-Mircheva and Lisa PascoeJul 20, 2022Jul 20, 2022
VeraExamining the Why and How of Integrating Your eTMF and CTMSAdapted from a Phlexglobal Ask An Expert interactive discussion held May 11, 2022, and available on-demand here.Jul 19, 2022Jul 19, 2022
