Regulatory affairs is a comparatively new profession which developed from the desire of governments to shield public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
Over the course of the last two years, fundamental changes have been made to the format and structure of regulatory affairs regulations, targeting demand and supply disproportion of the healthcare industry. From products, to processes, documentation to services, research to testing, manufacturing to packaging; all aspects of the industry are guarded by set of Govt. regulations.
The pharmaceutical, biotechnology and medical device research and development industries are among the most highly regulated industries globally. As pharmaceutical sector is growing rapidly, there is a need of regulatory affairs professionals to cater the current needs of industries for the global antagonism. Regulatory affairs professionals are the link between pharmaceutical industries and worldwide regulatory agencies. Pharmaceutical industry, being one of the highly regulated industries, is in immense need of people than ever before who are capable of handling issues related to regulatory affairs in a comprehensive manner
Cliniminds has been at the forefront of providing clinical research and pharmacovigilance training and consulting solutions to the life sciences industry for the last several years. We have already trained over 8,500+ professionals. All our programs are internationally accredited.