Preparing for the New Era: A Guide to Transitioning Clinical Trials to CTIS Regulation in the EU
Read the insightful article on transitioning to the CTIS portal authored by Bhuvaneswari Sivaraman, Regulatory SME, Regulatory Operations, Ragini Tushar Bhandari, Senior Manager, Regulatory Operations and Velkumar Kuzhandhaipandian, Senior Manager, Regulatory Operations and published in World Pharma Today. A leading online pharma digital platform, in May 2023.
Fill the form and download the article to learn more about
- What is the Clinical Trial Information System
- The Vital Prerequisites for Accessing the CTIS portal
- Key Benefits of Utilizing the CTIS portal
- Getting Authorization Right
Published by World Pharma Today
May 2023
![]() | Bhuvaneswari Sivaraman Regulatory SME, Regulatory Operations Navitas Life Sciences | ![]() | Ragini Tushar Bhandari Senior Manager, Regulatory Operations Navitas Life Sciences | ![]() | Velkumar Kuzhandhaipandian Senior Manager, Regulatory Operations Navitas Life Sciences |
© 2023 Navitas Life Sciences | Privacy Policy