Managing Global Regulatory Complexity
Clinical Trial Transparency, Reporting and Real-Time Data Driven Compliance
The complexity of global pharmaceutical regulatory management is both painful and multi-faceted having impact on both clinical and regulatory departments. Health Authority requirements for more transparency from sponsors and investigators has shaped the demand for open publication of clinical trial data.
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 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, Clarivate Analytics will share practical insights and provide details into:
- Best practices for managing global disclosure and resources
- How to improve efficiency in comparing regulatory requirements across countries
- How to increase harmonization, collaboration and communication between trial sites (Investigator), CROs (if delegated), sponsor, and MoH
- The bottom line impact of adopting regulatory best practices and technological innovation
This webinar event can help you, your team and organization to manage the complex regulatory landscape with greater competitive advantage, data driven insights and increased ROI. Don’t miss this event, register today.