tranScrip
Karen Real has extensive experience in the pharmaceutical industry, particularly in regulatory affairs. Karen has been the Director of Regulatory Affairs at Real Regulatory Ltd since January 2002 and has shown expertise in development strategy and managing virtual teams for the regulatory development, approval, and lifecycle management of medicinal products in Europe. Karen also has a strong network within the pharmaceutical industry and actively contributes to the regulatory sub-group of the UK's Ethical Medicines Industry Group. Additionally, Karen is the Founder and Senior Vice President of Business Development at tranScrip since April 2023.
Karen Real received their Bachelor of Science (B.Sc.) degree in Chemistry from the University of Galway, where they studied from 1987 to 1991. Karen obtained additional certifications, including being a Fellow of the Royal Society of Chemistry from December 2021 and a RAPS Member from November 2013 through the Regulatory Affairs Certification Program.
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tranScrip
tranScrip is a leading contract drug development organisation which supports pharma and biotech companies in the development and lifecycle of medicines. We bring innovative solutions to clients’ global drug development needs. From translational medicine through to registration and post licencing, we deliver both strategic leadership and operational execution of development programmes, covering clinical, regulatory, drug safety, and commercial elements. Our teams of physicians, scientists and regulatory experts, help clients select the most promising drug candidates and bring them to the market. We guide our clients through their decision making from first in man studies to proof of concept and pivotal trials, regulatory submissions and product launches. In the last decade, tranScrip has supported over 250 clients and has been integral to many development programmes and regulatory submissions, bringing products to the market each year across a wide range of therapeutic areas.