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OverviewFull Product DetailsAuthor: Phil Ambery (Global Clinical Head, Global Clinical Head, AstraZeneca, Gothenburg, Sweden) , Adrian Kilcoyne (Chief Medical Officer, Chief Medical Officer, Cellectis, New York, USA) , Daniel O'Connor (Director Regulatory and Early Access Policy, Director Regulatory and Early Access Policy, The Association of the British Pharmaceutical Industry (ABPI))Publisher: Oxford University Press Imprint: Oxford University Press Edition: 2nd Revised edition Dimensions: Width: 10.20cm , Height: 2.40cm , Length: 18.10cm Weight: 0.414kg ISBN: 9780198842255ISBN 10: 0198842252 Pages: 640 Publication Date: 04 December 2025 Audience: General/trade , General Format: Part-work (fascículo) Publisher's Status: Active Availability: Available To Order We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsReviewsAuthor InformationPhil Ambery is a Global Clinical Head in AstraZeneca, Gothenburg, Sweden. He leads clinical development of drug projects from phase 2 to launch in the cardiovascular, renal, metabolic and liver space. Over more than 20 years in Pharma he's led more than 10 clinical projects, first in GSK and now in AZ. He's passionate about teaching and education in pharma medicine and in the NHS, is a GMC associate and dual fellow of the college of physicians and faculty of pharmaceutical medicine. Adrian Kilcoyne has led drug development programmes across a range of projects in the past 20 years. He brings a wealth of experience as an editor of the handbook, having worked across diverse therapy areas and both small and large pharma. Adrian holds an MBA as well as a range of postgraduate medical qualifications. Daniel O'Connor is medically and PhD qualified and currently the Director Regulatory and Early Access Policy at The Association of the British Pharmaceutical Industry (ABPI). He joined the ABPI after 16 years at the Medicines and Healthcare products Regulatory Agency (MHRA). At the MHRA he was Deputy Director of the Innovation Accelerator and Regulatory Science. Dan has special interests in drug development, rare diseases, regulatory science, early access and health innovation. He previously held a Clinical Lecturer post at UCL and completed higher medical training in Pharmaceutical Medicine. Tab Content 6Author Website:Countries AvailableAll regions |
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