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Melina Cioffi
Melina Cioffi
VP, Regulatory Affairs | Aquestive Therapeutics
Morristown, New Jersey, United States
Melina Cioffi
Summary
Melina Cioffi is a seasoned Regulatory Affairs professional with over 20 years of experience in the pharmaceutical industry, focusing on all phases of product development. Currently serving as the VP of Regulatory Affairs at Aquestive Therapeutics, she has a proven track record in developing and executing global regulatory strategies and leading successful FDA interactions. Melina is known for her detail-oriented approach and her ability to manage complex projects involving clinical development and regulatory submissions. With a strong foundation in both clinical pharmacology and toxicology, she has played pivotal roles in various drug development initiatives across multiple therapeutic areas, including neuroscience and oncology. Fluent in English and Spanish, Melina brings a diverse perspective to her work, enhancing her communication and collaboration skills in international settings. She is passionate about advancing regulatory practices and ensuring the safety and efficacy of new therapies.
Melina Cioffi
Work Experience
VP, Regulatory Affairs at
Aquestive Therapeutics
August 2020 - Present
Head Of Regulatory Affairs at
Axsome Therapeutics, Inc.
March 2020 - August 2020
Director, Regulatory Affairs at
Forest Laboratories (now Allergan)
October 2014 - December 2018
Associate Director Regulatory Affairs at
Forest Laboratories
January 2012 - September 2014
Assistant Director, Regulatory Affairs at
Forest Laboratories
May 2010 - December 2011
Regulatory Affairs Senior Manager at
住友ファーマ
May 2008 - May 2010
Post-Doctoral Fellow (Manager-level role) at
Novartis
July 2006 - May 2008
Externship at
FDA
November 2005 - January 2006
Intern at
McNeil Consumer Healthcare
May 2003 - December 2004
Melina Cioffi
Education
University of the Sciences in Philadelphia, Doctorate
January 2000 - January 2006
Frequently Asked Questions about Melina Cioffi
What is Melina Cioffi email address?
Melina Cioffi's primary email address is *******@aquestive.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Melina Cioffi work for?
Melina Cioffi is a VP, Regulatory Affairs at Aquestive Therapeutics, a company specializing in Biological products, except diagnostic.
Where Melina Cioffi graduated from?
Melina Cioffi holds a degree in Pharmacy from University of the Sciences in Philadelphia.
How can I directly contact Melina Cioffi?
To contact Melina Cioffi directly, you can use the email address *******@aquestive.com. Complete contact information is available upon registration with Muraena.
Who is Melina Cioffi?
Melina Cioffi is a seasoned Regulatory Affairs professional with over 20 years of experience in the pharmaceutical industry, focusing on all phases of product development. Currently serving as the VP of Regulatory Affairs at Aquestive Therapeutics, she has a proven track record in developing and executing global regulatory strategies and leading successful FDA interactions. Melina is known for her detail-oriented approach and her ability to manage complex projects involving clinical development and regulatory submissions. With a strong foundation in both clinical pharmacology and toxicology, she has played pivotal roles in various drug development initiatives across multiple therapeutic areas, including neuroscience and oncology. Fluent in English and Spanish, Melina brings a diverse perspective to her work, enhancing her communication and collaboration skills in international settings. She is passionate about advancing regulatory practices and ensuring the safety and efficacy of new therapies.
Melina`s contact details
*******@aquestive.com
*************@allergan.com
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