David Lust is a Retired at Freelance. He possess expertise in regulatory affairs, pharmaceutical industry, regulatory submissions, gmp, fda and 22 more skills. He is proficient in English. Colleagues describe him as "David joined my former company to lead the RA CMC group in which I worked. He brought tremendous commercial and development experience to our group. He’s managed large international compliance projects, early and late stage development and registration products. He encouraged our team to think innovatively and guided us through many complicated strategies for both new product submissions and post approval changes. He empowered the team at every opportunity, making sure the technical teams recognized the RA CMC team leads. He taught me how to successfully transition from individual contributor to group leader. He has been a great mentor for me since we have moved on to other companies. " and "I have worked with Dave at Bristol-Myers Squibb, in various capacities, and Valeant (now known as Bausch Health), as a member of their Regulatory Affairs group. Dave is an extremely knowledgeable and diligent individual. He has the ability to quickly assess a situation and provide insight and possible solutions in a short period of time. He possesses good leadership skills while being open to alternative strategies. I highly endorse Dave for leadership roles in the pharmaceutical industry."