ThePharmyard MedDRA : Medical Dictionary for Regulatory Activities
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Products In Euromed (Total Products 79, Showing: 1 -> 20)
Advanced laser technologies in medical device manufacturing Advanced laser technologies in medical device manufacturing
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Reprinted from the Medical Devices Manual, Andrew May explains how laser welding, cutting, marking and surface treatment are opening up new opportunities for companies to meet the needs of surgeons and of course, ultimately - patients.
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Animal materials and derivatives in medical devices Animal materials and derivatives in medical devices
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Reprinted from the Medical Devices Manual and written by Brian Matthews, this expert review explores the potential issues which may arise from the use of animal materials and their derivatives.
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Application of Nanotechnologies for Medical Devices Application of Nanotechnologies for Medical Devices
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The first applications of the nanorevolution in medical products have already started to reach the market. David Farrar explains some of the key nanotechnologies that are likely to impact on medical devices and issues involved in their development.
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Benchmarking in the pharmaceutical industry Benchmarking in the pharmaceutical industry
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Reprinted from the Clinical Research Manual, Alison Drasdo explains how by providing baseline comparisons, benchmarking can highlight where improvements may be possible and thus most importantly provides the momentum for change.
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Branding pharmaceuticals Branding pharmaceuticals
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Reprinted from the Medical Marketing Manual, Mike Rea explains that there are many definitions of a ‘brand’, however because a brand is, by its nature, conceptual and intangible, it remains difficult to point to, to touch, to feel.
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Canadian regulations for medical devices Canadian regulations for medical devices
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Reprinted from the Medical Devices Manual Bernard Tremaine addresses the main regulatory issues concerning the placing of or making available for sale, medical devices on the Canadian market.
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Case studies in pharmacoeconomics and assessment of outcomes Case studies in pharmacoeconomics and assessment of outcomes
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Written by Professor David Sclar this is chapter 5 from the book Pharmacoeconomics and Outcome Assessment: A Global Issue, Edited by Dr Sam Salek, University of Wales, Cardiff.
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China Medical Devices Regulatory Overview China Medical Devices Regulatory Overview
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Reprinted from the Medical Devices Manual Jack Wong guides you through the classification and regulations for medical devices in China and Hong Kong, which although part of China, has a different regulatory system.
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Choosing a CRO: The Foundation of a Successful Partnership Choosing a CRO: The Foundation of a Successful Partnership
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Reprinted from the Clinical Research Manual, Kenneth Getz explains that CROs now play a common yet integral role in all aspects of clinical trial management, from protocol design through post-marketing surveillance.
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Clinical Research for Medical Devices Clinical Research for Medical Devices
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Reprinted from the Medical Devices Manual, Lucio Fumi describes how attitudes towards clinical research in the medical device industry has always been different from those prevalent in the pharmaceutical industry, for a number of reasons.
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Clinical trials - pre and post launch Clinical trials - pre and post launch
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Reprinted from the Medical Marketing Manual, Jane Baguley describes how pharmaceutical companies invest hugely in the conduct of clinical trials to meet regulatory requirements, secure marketing authorisation and monitor safety thereafter.
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Clinical trials in Central and Eastern Europe Clinical trials in Central and Eastern Europe
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Reprinted from the Clinical Research Manual, Jean-Pierre Tassignon discusses patient recruitment, site productivity, cost-effectiveness and data quality in this geographical area.
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Clinical Trials in China Clinical Trials in China
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Reprinted from the Clinical Research Manual, Dr Gamal Hammad and Professor A. Kamel Mashhour explain how all prescription-only medicines (POMs) must be subjected to local clinical studies prior to local marketing approval.
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Clinical Trials of Medicines in Children Clinical Trials of Medicines in Children
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Reprinted from the Clinical Research Manual, Professor Imti Choonara explains how clinical trials of medicines in children are more difficult than corresponding studies in adults. However, they are by no means impossible.
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Combination of drug and device in needlefree injectors Combination of drug and device in needlefree injectors
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Reprinted from the Medical Devices Manual and written by Roger G Harrison, this expert review summarises some of the data that are currently available and will project the future applications and place of needle-free injection.
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Commercial input into development plans Commercial input into development plans
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Reprinted from the Medical Marketing Manual, Philip Blake explains that the main goal of any Product Development (PD) unit is to increase the value of the product portfolio.
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Commercial input into development plans Commercial input into development plans
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Reprinted from the Clinical Research Manual, Philip Blake discusses the key benefits of commercial input into all stages of development, research priorities and working with regulatory and clinical to optimise the final labelling.
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Commercialising products for medical professionals; bridging the cultural divide Commercialising products for medical professionals; bridging the cultural divide
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Reprinted from the Medical Marketing Manual, Mike Rea explains that although ‘medical’ and ‘commercial’ interests seem to sit at separate ends of a spectrum, most participants are comfortable with a degree of commercialism in their practice.
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Conference marketing: events, exhibitions and sponsorship Conference marketing: events, exhibitions and sponsorship
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Reprinted from the Medical Marketing Manual, Mike Rea argues that ‘Conference marketing’ is set to remain a central feature of every pharmaceutical brand plan, despite the explosion of Internet-based physician contact.
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Confronting the challenges in developing a biosimilar medicinal product Confronting the challenges in developing a biosimilar medicinal product
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Reprinted from the Clinical Research Manual, Cecil Nick discusses the legal basis for a biosimilar medicinal product in the EU, the regulatory guidelines and partnering with a CRO.
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