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trialscope disclosure workshop

Last-minute, late, and overdue clinical trial disclosures put your organization at risk for non-compliance, fines, and an erosion of public and investor trust.Provide your teams with the industry awareness and the tools they need to maintain compliance – and keep your organization out of trouble. Tap into insights from TrialScope’s Disclosure Workshops.

Each workshop covers a different area, empowering your teams to successfully navigate new compliance regulations while easing the burden of performing disclosure tasks. 

Register for one, two, or all sessions, and enjoy a complimentary Lunch and Learn covering the history, trends, benefits, and risks associated with clinical trial disclosure and compliance. 

Equip your teams with the right disclosure knowledge

Discover best practices for integrating plain language summary (PLS) preparation throughout the clinical trial lifecycle. Provide patient transparency from study planning and protocol development through to results and PLS postings.
Transform your clinical trial documents into redaction-ready materials as part of your day-to-day study planning and operations. Adopt these standardized rules for preparing, anonymizing, and submitting documents. Learn from and take advantage of the experts in preparing for Health Canada PRCI submissions, EMA’s Policy 0070 and more.
Promote transparency internally and externally by creating and adopting unified policies and processes tailored to your organization’s specific disclosure procedures.

Next steps

Getting a demo tailored to your needs is the best way to see how our solutions will help you gain an advantage.

Request live demo now:

Our team is ready to hear from you for a particular request or area of interest. Please do not hesitate to reach out and discuss.

Contact us for product technical and account support.

  • US Toll-Free   : +1 888 670 8900 
  • US Toll             : +1 212-600-3520
  • UK & Europe : +44 (0) 208 052 0700

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