CSA intends to provide recommendations to life sciences companies on computer software assurance for computer systems and automated data processing systems that are part of medical device production or the quality system.

Get trained in Regulatory affairs from one of the best institute in India.

Drug Regulatory Affairs refers to all aspects within the pharmaceutical development process and how they are subject to various degrees of regulation.

Medical writing involves creating well-structured scientific documents that include clinical research documents, content for healthcare websites, health magazines, journals and news.

As per a recent analysis by Emergent Research, the Pharmacovigilance market is expected to be valued at $12 billion by 2027, an indication of rapid growth in the sector post COVID.