End-to-End Management of Regulatory Processes and Digital Trust in the Drug Lifecycle
End-to-End Management of Regulatory Processes and Digital Trust in the Drug Lifecycle
The pharmaceutical sector is one of the most heavily regulated globally. Digitalization in the life science sector can be complex due to specific challenges related to regulatory compliance. On the other hand, this stringent regulation is essential to ensure the safety, efficacy, and quality of products and services provided in the medical, pharmaceutical, and biotechnological fields.
How can we not miss significant opportunities to improve efficiency, accelerate product development, and enhance overall quality with digital solutions?
Certainly, with the help of partners who understand the sector's specific needs and current regulations.
EXTEDO and INFOCERT - Register for an exclusive webinar on 14 March (held in Italian)
EXTEDO and INFOCERT are delighted to invite you to a joint webinar to show you how easy it can be to digitize the entire drug lifecycle in a fully compliant manner. Together we have organized a live session to demonstrate the functionality of EXTEDOpulse, managing every phase of pharmaceutical product development through integration with InfoCert's Trust solutions.
Register now and learn how your organization can approach the future of submissions. Secure your spot in this outstanding event and receive the recording!
Discover the agenda and reserve your spot on 14 March 2024, 16:00 CET, 60 Minutes
Please Note: The webinar will be held in Italian!
Agenda
- EXTEDO and INFOCERT Collaborating for Trust and Compliance in Pharma Processes
- EXTEDOpulse Live Demo
- Regulatory activity planning
- Registration content planning
- Automatic compilation
- Documentation review
- GOSIGN Live Demo
- Approval Workflow Management
- Quickstart module for external user signatures
- Compliant document archiving
- Q & A Session