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As per available reports about10 relevant journals, 71 Conferences, 6 workshops are presently dedicated exclusively to Government Affairs and about 1543 articles are being published on Government Affairs.
A regulatory affairs (RA), also called Government affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, banking, telecom etc. A government affair also has a very specific meaning within the healthcare industries (pharmaceuticals, medical devices, biologics and functional foods).Government affairs professionals usually have responsibility for the following general areas Ensuring that their companies comply with all of the regulations and laws pertaining to their business. Working with federal, state, and local regulatory agencies and personnel on specific issues affecting their business. Biologics and Other Novel Therapies, Drug Designing And Development
OMICS International Organizes 1000+ Global Events Every Year across USA, Europe & Asia with support from 1000 more scientific societies and Publishes 700+ Open access journals which contains over 100000 eminent personalities, reputed scientists as editorial board and organizing committee members. The conference series website will provide you list and details about the conference organize worldwide.
Scope and Importance
Government affairs Conference provides the scope for opportunities to learn progressed by international scientists and academicians. Government affairs also called Regulatory affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, banking, telecom etc. A government affair also has a very specific meaning within the healthcare industries. Government Affairs Conference offers excessive quality content to suit the diverse professional development. It is a perfect platform to discuss the current discoveries and developments in the field of Regulatory affairs.
The market was valued at US$1.56 billion in 2013 and is estimated to reach a value of US$4.49 billion by the end of 2020.With the help of regulatory affairs outsourcing, life science, pharmaceutical, and medical device manufacturing companies are able to get their drugs or devices approved or launched in the global market. Regulatory affairs outsourcing by biopharmaceutical companies has minimized losses due to recalls and product approval delays. Regulatory affairs service providers also provide effective services such as clinical trial services, medical writing, and pharmacovigilance to biotech, pharma, and medical device companies.
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This page was last updated on 14th Sep, 2015
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