Dennis Nosco, PhD, RAC
University of Cincinnati
Tell me more about Dennis Nosco, PhD, RAC?
Dennis Nosco, PhD, RAC is a highly experienced regulatory affairs professional with over 43 years of work experience. He has a strong background in regulatory affairs, FDA regulations, and clinical trials. Throughout his career, he has worked with Certus International and independently with clients, developing regulatory review processes and training. Dennis has extensive expertise in drug discovery and development, clinical studies, and CMC regulatory. He holds a PhD in Chemistry and is RAC certified in US regulatory affairs.
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I am a regulatory affairs professional, specializing for the last 19 years in regulatory review of pharmaceutical advertising and promotion (including 3 major drug launch campaigns) with the last 7 years being as a consultant working with Certus International and independently with clients. I have both US and O-US experience in ad/promo review, have developed regulatory review processes and done internal trainings as both an employee (Mallinckrodt) and as a consultant. I have been invited to speak multiple times at both the annual DIA and FDLI pharmaceutical advertising meetings. I also have extensive pharmaceutical experience in allied areas including drug discovery and development (23 US patents and over 30 peer-reviewed scientific publications), clinical studies (working as both a CRA and in Medical/Clinical) and CMC regulatory and have some experience in target product profiles, company core data sheet development, manufacturing and in QC, all of which aid in my ability to review promotional pieces and help with promotional strategies. I hold a PhD in Chemistry and am RAC certified in US regulatory affairs.
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president nosco consulting llc dnosco@hotmail com
President
Mining
Dennis Nosco, PhD, RAC's Professional Milestones
- President (2014-05-01~2016-01-01): Driving strategic direction and achieving record-breaking revenue growth through strategic leadership.
- Sr. Director, Global Labeling, Regulatory Affairs (2012-01-01~2014-04-01): Implementing comprehensive labeling guidelines, ensuring compliance with global regulations, and ensuring fair and transparent trade agreements.
Education
Inorganic Chemistry
1975-1980Skill
Regulatory Affairs
Fda
Pharmaceutical Industry
Clinical Trials
Life Sciences
Biotechnology
Regulatory Submissions
Commercialization
Pharmaceutics
Technology Transfer
Clinical Development
U.s. Food And Drug Administration
Regulatory Advertising And Promotion Review
Strategic Planning
Oncology
Sop
Healthcare
Standard Operating Procedure
Drug Development
Medical Devices
Certification
Colleagues
M.haroon Zareef
President
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