The path to approval is littered with pitfalls leading to unnecessary delays getting your medicine to the people who need it the most….the patients.
With over 25 years experience from the Life Science industry and through her numerous interactions with both the FDA and European agencies, Dr. Laurie Smaldone Alsup is perfectly positioned to help you resolve the issues that could cost you time, money and potentially, approval.
Steps to success
Step 1: Identify your most difficult strategic regulatory question in the US or European market.
Step 2: Click on the link below and schedule a complimentary 30 minute session with Dr. Laurie Smaldone Alsup, CMO/CSO NDA Group and Advisory Board member.
Step 3: Receive valuable regulatory insights into your drug development program that will save you significant time and money.
Where: BIO International Convention in Philadelphia
When: 3 – 6 June 2019
Book a meeting: firstname.lastname@example.org