– May 26th, 2021 –
During this webinar, learn how Janssen Pharmaceuticals used an innovative technology approach to increase both agility and compliance in their Critical Document Review Processes.
- How Medical Affairs, Commercial and Market Access teams can use workflow automation to reduce compliance issues across approval processes
- How to streamline review processes to accelerate time to market
- The importance of collaborative document authoring for better content quality
Webinar Summary
In a rapidly evolving environment for Pharma, leaders who can accelerate time to market while balancing compliance mandates will excel. But balancing the need to be more agile while grappling with greater regulatory oversight is an increasing challenge.
What role can technology play in helping to balance these seemingly contradictory goals? During this webinar, learn how one of the largest pharmaceutical companies in the world used an innovative technology platform to achieve this balance in their Critical Document Review Processes.
Click here for more information and to register.
