This week the ClaritiDox team attended DIA in Virginia!?Some of our?T&D experts,?Brenda Tiffin,?Brodie Barnard?and?Gregory Shear?had the opportunity to discuss?topics such as?US and EU Disclosures, Policy 0070, CTIS submissions and CCI protection. Also, it was great to connect with clients and colleagues!?Be sure to connect with ClaritiDox LLC for more information on how our T&D services can support your team.
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Experience and great people matter. Our outstanding team of writers, editors and redactors is here to support you. Clinical Trial Registration | Third Country Protocol Registration | Clinical Trial Results Disclosure | ClinicalTrials.gov | EU Clinical Trial Registry | Health Canada | Anonymization | Plain Language Summaries | Medical Writing and Publications | Quality Control |
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https://www.ClaritiDox.com
ClaritiDox LLC的外部链接
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ClaritiDox LLC员工
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This week the ClaritiDox team attended DIA in Virginia!?Some of our?T&D experts,?Brenda Tiffin,?Brodie Barnard?and?Gregory Shear?had the opportunity to discuss?topics such as?US and EU Disclosures, Policy 0070, CTIS submissions and CCI protection. Also, it was great to connect with clients and colleagues!?Be sure to connect with ClaritiDox LLC for more information on how our T&D services can support your team.
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It's an all-pro panel on PLS at Citeline’s TrialScope EXTRA in New York City — Maureen Kashuba, Merck Associate Director,?CDD&T, Leading Health Literacy Projects?and Plain Language Summaries; Julie Holtzople, ?President of Holtzople Consulting; and Courtneay Parsons, Head of Plain?Language Summaries at?ClaritiDox — moderated by Sylvia Baedorf Kassis, MPH, CYT, Program Director, Multi-Regional Clinical Trials Center (Multi-Regional Clinical Trials Center of Brigham and Women's Hospital and Harvard (MRCT Center) of Brigham and Women's Hospital and Harvard. #clinicaltrials #PLS #disclosure #trialscope #plainlanguagesummaries
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Don’t miss this!
LIVE WEBINAR: Thursday, February 22nd at 10am EST Commercially Confidential Information: Why It’s So Hard and What You Can Do To Streamline CCI In Your Organization. Lessons learned from practical experiences with CTR and Policy 0070 projects During this webinar we will provide CCI insights gained from practical hands-on experience with dozens of CTR and Policy 0070 projects. We will also include summary survey results and perspectives from direct discussions with multiple trial sponsor transparency leaders and Health Authority interactions. This webinar is designed for those who are looking to improve upon the challenges associated with Confidential Information. Example questions that will be addressed include What type of information is most commonly redacted? What redactions may be more applicable for early stage trials? In what subject areas might there be a lot of potential CCI? Why? What are some of the least common redactions that sponsors have considered?
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I’m excited to be speaking at Clinical Data Disclosure Europe hybrid event on 6 – 7 November, 2023. Join me for 2 days of inspirational insights, discussion and exclusive networking with our expert clinical disclosure and dissemination community with 10% discount* using VIP code: CDDEUSPEAKER. Register your pass today and benefit from Authority guidance, industry case studies and practical advice: https://lnkd.in/gt-RKrCD . Informa Connect
Clinical Data Disclosure Europe 2023
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