Clarivate Analytics

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Managing Global Regulatory Complexity: Clinical Trial Transparency, Reporting, and Real-Time Data Driven Compliance

• Navigating global regulatory complexities requires simplification. • Technology can optimize daily activities and overall compliance. • Increasing transparency with real-time data provides more accurate insights.

Managing Global Regulatory Complexity: Clinical Trial Transparency, Reporting and Real-time Data Driven Compliance

Technology is enabling regulators from organizations of all sizes to process the large amounts of data available to them to make better, faster decisions and take regulatory action where needed and when. Join PharmaExec and Clarivate Analytics on August 14th, 2019 at 12 Noon EST for the webinar: Managing Global Regulatory Complexity: Clinical Trial Transparency, Reporting and Real-Time Data Driven Compliance. Guest Speakers: Robert Paarlberg, Principal of Paarlberg & Associates LLC, a consultancy specializing in global clinical trial disclosure strategy and operations, regulatory policy and regulatory intelligence, Teresa Fishburne, Director & Global Practice Lead, Clinical and Regulatory, Clarivate Analytics and April Hernandez, MSc., Regulatory Consultant, Live: Wednesday, Aug. 14, 2019 at 12pm EDT | 9am PDT | 5pm BST | 6pm CEST On demand available after airing until Aug. 14, 2020. Register free