BIOMEDevice Boston connects you with more than 4,500 engineers and executives — and more than 450 leading suppliers — across New England's thriving medtech industry. In partnership with the Massachusetts Medical Device Industry Council (MassMEDIC), BIOMEDevice Boston is a powerful end-to-end industry showcase covering today's emerging biomedical trends and innovations. Explore the full spectrum of cutting-edge solutions you need to...

Clinical Development Riding the iWave!Clinical OperationsTechnical OperationsPeri-Approval ResearchMedical WritingThe DIA Clinical Forum is widely recognised as the only European conference that brings together industry thought leaders across the key disciplines of data management, clinical operations, drug safety and medical writing. The conference shares experience, case studies, lessons learned and best practices with professional colleague...

Neutral, global forum featuring over 110 sessions attracting more than 3,000 professionals involved in the development of medicines from more than 50 countriesThe DIA's Annual EuroMeeting is global in scope and attracts well over 3,000 professionals from more than 50 countries. It brings together professionals from the biopharmaceutical industry, contract research and service organisations, academic research centres, regulatory agencies and he...

Patient safety is the biggest single issue in the NHS and UK healthcare. After a year of unprecedented focus on patient safety, 2014 is the start of the next stage in the journey to eradicate avoidable harm and deliver improved outcomes. The legacy of the Francis report (and the government’s formal response) into Mid Staffordshire, the Keogh review into trusts with unusually high mortality rates and the Berwick review on behalf of the Pr...

With the ability to measure multiple analytes with high sensitivity, often faster and more cheaply than other methods, mass spectrometry is becoming an attractive method of analysis for the clinic. Featuring an array of leading researchers and clinicians, SELECTBIO’s Clinical Applications of Mass Spectrometry conference aims to provide you with an insight into the latest developments in this area.As the analytical power of mass spec is r...

SELECTBIOs inaugural Food Analysis Congress aims to present the latest developments in food analysis technologies, in response to the increasing demand for rapid and efficient food safety and quality testing. Focus will be given to advances in both the analysis of natural food allergens and toxins, as well as contaminants introduced through processing and packaging. Points for discussion will also include the ongoing issue of food traceability...

This is the 4th DIA African Regulatory Conference (ARC) co-organised by the Drug Information Association (DIA) and the IFPMA’s African Regulatory Network (ARN). IFPMA (International Federation of Pharmaceutical Manufacturers and Associations) represents the researchbased pharmaceutical companies and associations across the globe. The research-based pharmaceutical industry’s 1.3 million employees strive to develop and provide innova...

This year's conference will focus on the current and future landscape of the biosimilars market and will allow input from key industry experts in the field to engage in meaningful and important discussions on how to accelerate drug development to market. Be part of a major networking opportunity providing intimate interaction with your peers, where you will hear case studies, presentations and round table discussions on the key issues surround...

New EU requirements are expected to come into force during 2014, impacting clinical trial processes including informed consent as well as the provision of public access to information and results of clinical trials. This workshop will review the new transparency requirements and voluntary commitments and, describe how these will impact current disclosure procedures. There will be a focus on sharing experiences on how the requirements are being...

This 2-day workshop will provide a forum for information exchange and discussion on conceptual and practical questions through lectures, panel discussions, and interactive break-out sessions. The new EU Clinical Trials Regulation is expected to become applicable in 2016. The new legislation will have implications on clinical trial sponsors preparing and submitting clinical trial applications. Member States will have to adapt their procedures f...