Subject Matter Expert Office Hours

December 9, 2021, 9:00 am - 1:00 pm

Event Details

Do you need help navigating a successful regulatory pathway? Schedule time with our LSWI Insider Advisors to get advice on your specific needs!

When developing a prescription drug product or medical device, it often feels as if the future of the company hinges on FDA approval. Companies seeking approval for must thoroughly understand the five-step process they must complete: discovery/concept, pre-clinical research, clinical research, FDA review and FDA post-market safety monitoring.  The regulatory approval process and FDA guidelines continue to evolve, so it’s important to work with experienced partners who can guide you to the fastest path to approval.

30-minute virtual sessions available with our regulatory expert advisors.


Email to reserve a spot!