Regulatory Agencies throughout the world are becoming increasingly critical and demanding of Trial Master File management and Vendor oversight. New industry guidelines, such as ICH-GCP E6 R2, are also impacting the way clinical trials are managed and executed. With this in mind, InClin and GSK are excited to announce their CRO and Sponsor Partnerships webinar!
Join our webinar on Achieving TMF Excellence: CRO and Sponsor Partnerships
Thursday, June 28, 2018 (7:00 am Pacific / 10:00 am Eastern)
Expect to hear lessons learned and recommendations for best practice as they deep-dive into common industry challenges such as:
- TMF completeness and cross-functional collaboration
- Vendor oversight and metrics
- Regulatory inspection, lessons learned
With expert insight, this hour-long presentation will shine a spotlight on best practices for exchanging Trial Master File (TMF) content. Take advantage of the opportunity to hear both the Sponsor and CRO perspective to ensure mutual expectations are achieved at the highest level of quality in your strategic partnerships.
Registration is FREE, and couldn’t be easier – so what are you waiting for? To register for the event click here: Register For The Webinar
InClin is a full-service Contract Research Organization (CRO) with offices in the San Francisco Bay Area and Sydney, Australia. We are a single source provider of an integrated full suite of clinical development services from Phase 1 through Phase 4, including project management, clinical monitoring, site and contract management, vendor management, data management, biostatistics, programming, drug safety, medical monitoring, medical writing, QA inspection readiness, as well as strategic consulting services. For more information feel free visit our website or contact us at our email address below.