GlobalInstituteofRegulatoryAffairs

  The medical device industries work in tandem with the pharmaceutical industries by providing innovative solutions to improve patient outcomes. The companies either innovate by updating the existing technology or developing a new device. These devices provide a means for the effective treatment of a particular disease or condition. A regulatory affairs professional performs a critical role in the medical device lifecycle-right from the innovation of the device to the device reaching the physician. It includes   medical device compliance training , leading premarket strategy, drafting regulatory submissions, and ensuring post-marketing compliance. As all of these activities are scrutinized, it demands a professional with a specific set of skills. If you wish to set your foot in this domain, here are the skills you need to watch out for: 1. Regulatory Knowledge Usually, a degree in any field of science with  regulatory affairs medical device courses  may pave the way into entry-level jo

  The Indian pharmaceutical industry is a success story providing employment for millions and ensuring that essential drugs at affordable prices are available to the vast population of this sub-continent. - Richard Gerster The Indian Pharma Industry has been growing at a rapid space in the last 4 -5 years, according to a McKinsey Report India Pharma 2015 the industry is expected to grow at a CAGR of 16% for the period of 2007-2011. The growth and development of Indian Parma industry has seen India on the world map, today India has gained the reputation of producing high quality low cost generics. Indian Pharma Industry has more than 20,000 registered units producing drugs. India also has the largest numbers of US FDA approved plants outside USA. India has become the favored destination for all sought of Pharmaceutical activities, out of this Research & development and Clinical Research are the front runners. This increase is Pharmaceutical activities has seen a major demand for ski