UNITED KINGDOM – Garry Mehrabian, MD Joins EASY GLOBAL TRAINING Team as Senior Medical Adviser

The growing trends of Clinical Trials demands a highly efficient training program for the team involved in different aspects of it. In this era of information with all kinds of data available in the cyber space, the task of browsing and selecting the appropriate credible material has become more difficult than ever. At EASY GLOBAL TRAINING, we are dedicated to eliminate this barrier by providing credible-peer-reviewed educational material to our audience with the added benefit of having experts with many years of industry experience to provide further support on a customized level that fits your needs.

We are delighted to announce that Dr. Mehrabian just agreed to join our team of world-wide consultants and advisers and will be collaborating with us out of the UK. Dr. Garry Mehrabian is a Medical affairs / Drug safety expert with more than 25 years of experience in pharmaceutical / CRO industry. At the moment, he is the Senior Director (Medical Affairs / Drug Safety) at Neometrix Consulting Inc. He is a medical doctor who gained his experience working within clinical, medical affairs and pharamcovigilance roles as medical advisor, medical monitor, drug safety physician, clinical research physician and medical director. His experience covers many major therapeutic areas, including: Oncology, Haematological Malignancies, Cardiovascular, CNS, Anti-Infective / HIV, and Immunology. The roles he has hold in the past include: Medical Monitor at BAYER, Germany; UCB-Celltech, UK; i3 Research, UK; Cmed, UK; Neometrix Consulting, Canada; Drug Safety Physician at PAREXEL, UK; Johnson & Johnson, UK; i3 Research, UK; Eisai, UK; Chiltern, UK; Neometrix Consulting, Canada; Senior Medical Adviser / Clinical Research Physician at GSK, UK; UCB Celltech, UK; Medical Director Oncology at i3 Research, UK; Neometrix Consulting, Canada; Medical Director PVG at i3 Research, UK; and Global Director PVG at  Chiltern, UK. Dr. Garry Mehrabian, is specifically addressing our clients needs in the fields of Drug safety/Pharmacovigillance, Medical monitoring, Medical Affairs, and providing Medical Advice in a wide range of therapeutic areas and both fro Drug Development and Medical Device companies covering both US and EU presence.

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Easy Global Training is based in Bethesda, MD in the United States. It is a leading, up-to-date information network in the fields of Regulatory Affairs, quality compliance, and medical affairs for life sciences (drugs, excipients, devices, and combination products), food  & food ingredients, dietary supplements, and complementary / alternative medicine. Our portfolio of products includes webinars (live and on-demand), e-learning self-paced modules, in-class training, white papers, e-books, guidelines, best practices, reports, job aids, and e-newsletters. We also provide social media channels with webcasts and interviews from the industry experts, as well as academic and regulatory body experts on regulatory training and quality compliance hot topics, best practices (GMP, GDP. GCP. GLP. GVP, …), guidelines, and regulations at a global level. For your convenience, we also provide a variety of forms and templates across these fields. Easy Global Training strives to provide a wide network of high-quality resources that are up-to-date and to communicate new updates as well as new insights and competitive points of view. This is a collaborative platform, designed for professionals across a variety of fields to learn and share valuable information related to the latest laws, policies and regulations, while ensuring continuous improvement in global operations, regulatory training, quality compliance, and safety.