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Leaders in regulatory excellence

Our regulatory specialists take active roles in shaping key industry bodies including the European and United States Pharmacopoeia, EXCiPACT™ and IPEC. They represent our dedicated Health Care Manufacturing sites and act as the link between the Health Care business, the regional manufacturing sites and regional sales teams. Extensive experience in the submission and progression of new monographs and teams experience in supporting the use of novel and innovative pharmaceutical products in customer formulations had a particular role to play in the recent success of our business.
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Jette Kjeldal,

Jette Kjeldal, MBA

Quality and Regulatory Assurance Director for Croda Health Care

Jette Kjeldal, MBA, Quality and Regulatory Assurance Director for Croda Healthcare is located at our Vaccine Adjuvant site at Frederikssund in Denmark. With more than 25 years of work experience in the Life Science Industry she has profound experience with Product Development, Manufacturing, Quality Control and Assurance under GMP for excipients, Active Pharmaceutical Ingredients, sterile and non-sterile Medicinal Products (EU GMP Part I and II) and Medical Devices for In Vitro Diagnostics (ISO13485). She possesses an extensive knowledge about quality systems and processes, product filings, as well as a proven business and leadership track record.
Miquel Mir,

Miquel Mir

Global Quality & Regulatory Mgr. – Pharma Excipients

Miquel has a Ph. D in Organic Chemistry and joined Croda (Uniquema) 20 years ago as the European Technical Service Manager for Health Care. Since then, he worked in different positions on the areas of Quality and GMP’s, Regulatory Affairs and Product Development. He has been a member of the Ph. Eur. Group of Experts 13H (fatty acids and derivatives) during the period 2004-2008. At the current position as the Global Quality & Regulatory Manager-Pharma Excipients he is working on assisting customers, global Sales and Site quality teams making excipients with respect to QA and RA matters. His work contributes to the development of the business for the Health Care Segments Pharmaceutical Excipients, Human Vaccines and Consumer Health by helping to meet the high expectations of the pharmaceutical industry about the quality and regulatory requirements of our products.
 
Lonna Tucker

Lonna Tucker

Executive Director of Regulatory Affairs and Compliance at Avanti Polar Lipids

Lonna TuckerExecutive Director of Regulatory Affairs and Compliance at Avanti Polar Lipids, works with numerous clients and products to provide support for regulatory filings at all phases of development, including commercialization. This includes drug master file authoring, editing, and coordination of information provided by subject matter experts. Drug Master Files are prepared and submitted in electronic Common Technical Document (eCTD) format. Submissions are supported primarily in the United States, Canada, and the European Union but submissions in other countries are also included. Interaction with Health Authorities and knowledge of global regulations are key components of Avanti’s regulatory department. Lonna has held Regulatory Affairs Certification (RAC, US) since 2011.
Dr Richard Cawthorne

Dr Richard Cawthorne

Research and Technology Fellow

Dr Richard Cawthorne, Research and Technology Fellow, sits on the United States Pharmacopeia’s Excipients Expert Committee. Richard says “My involvement in the Committee allows us to initiate new monographs and gives us input into significant revisions of existing monographs. This means we are playing a lead role in developing new standards that will help our customers.” Richard is a member of the European Pharmacopoeia’s Fatty Oils and Derivatives expert group, whose work programme encompasses the monographs that apply to over 200 of our excipients.

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