Nottingham, U.K, (19 March 2013) –Quotient Clinical, part of Quotient Bioresearch (“Quotient”) today announced that three new pharma and biotech clients have selected its RapidFACT service to support the development of optimal drug products for pulmonary, transdermal, and ocular administration. This marks a key extension in the application of RapidFACT across a wide range of dosage forms and delivery routes.
RapidFACT (Rapid Formulation development And Clinical Testing) is underpinned by a Translational Pharmaceutics platform that integrates formulation development, “real-time” GMP product manufacturing, and clinical testing. Compared to conventional development processes, RapidFACT shortens development timelines, lowers costs, and also reduces the consumption of drug substance by up to 90%.
Mark Egerton, Managing Director of Quotient Clinical, said: “We are delighted that RapidFACT has been selected to support the development of these exciting new products. To date, RapidFACT has been deployed on over 30 programs that have focused on oral delivery or intranasal delivery. These new programs further demonstrate the broad utility of RapidFACT and our belief that it can be used to support the development of molecules for any route of delivery.”
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Tel: 0115 948 6900
About Quotient Clinical
Quotient Clinical, part of Quotient Bioresearch, “Quotient”, has over 20 years’ experience delivering high quality data to provide innovative early drug development solutions to pharmaceutical and biotechnology clients worldwide, including 17 of the top 20 pharmaceutical companies. Our expertise in Exploratory Clinical Pharmacology, Drug Product Optimisation, and 14C Enabled Drug Development, underpinned by our unique Translational Pharmaceutics™ and Synthesis-to-Clinic™ delivery platforms, adds significant value to client development programs.
For further information, visit www.quotientbioresearch.com/clinical.