BDD – delivering the impossible for our clients.
BDD combines drug delivery expertise and clinical capabilities to accelerate product development pipelines, enable life cycle management and create new value-added products. Rapid parallel clinical testing with BDD SWIFT significantly reduces the time from product concept to clinical success.
Prove your product claims with BDD Scintigraphy, best in class scintigraphic clinical trials.
A unique patented time release technology, OralogiK™ provides unrivalled control of drug release at the right place and the right time to achieve a superior and clinically effective drug delivery profile.
BDD SWIFT for rapid clinical development. SWIFT accelerates evaluation and optimisation of product performance using in vivo clinical data to direct formulation design in real time. SWIFT studies enable you to make decisions on formulation changes based on emerging clinical data. This integration of formulation development, GMP manufacturing and clinical testing activities can reduce the time from initial prototype development to clinical results to just 6 months.
BDD aims to be the number one integrated pharmaceutical development centre. Because we recognise that one size does not fit all we specialise in providing responsive, flexible and innovative solutions to our customers.
Our success is built upon solid scientific ability, strengthened by shared values across the company. Our commitment to our clients is at the forefront of everything we do; we always keep our promise and deliver when we say we will. We are a company of integrity and value and we take pride in everything that we do.
Howard Stevens Chairman
Professor Howard Stevens is a registered pharmacist whose career spans four decades of management of industrial research and development in the UK and Europe in large multinationals and small drug delivery companies. He has been involved in the formation of several successful spin-out businesses and served as the Pfizer Professor of Drug Delivery at the University of Strathclyde from 1998-2009. He has an extensive scientific and patent publication record, is a fellow of the RPSGB, RSC and APSGB and served as Chairman of the APSGB in 2001
Dr Carol Thomson has had a varied career in management in the science sector and developed strong operational management and leadership skills at Thomson Reuters, where she managed the Pharmaceutical Patents Business Unit of the World Patents Index. Following this, Carol spent three years at the University of Strathclyde in a Research Business Development role and subsequently as Research Policy Manager. Carol has a degree in Genetics and PhD from the University of Sheffield.
Glenn Crocker MBE Non-Executive Director
Dr Glenn Crocker has a first degree in Genetics and a DPhil in Immunology from Oxford University. He qualified as a chartered accountant with Ernst & Young and worked in the life science practice for a number of years where he focused on advising the biotechnology industry, spending several years in Palo Alto, California, and returning to Cambridge to head the UK biotechnology practice for the firm, focusing on business development and corporate finance transactions.
Joanne Kelley has a long and extensive experience of global commercial and general management in the pharmaceutical industry and has led a range of transactions including M&A, technology licensing and collaboration arrangements. Previously in her role as Vice President of Business Development, Head of Transactions at AstraZeneca, Jo was responsible for a number of transformational deals and has received a number of awards recognising her deal making achievements from colleagues and peers, including recognition from The Pharmaceutical Licensing Group.