Electronic Signatures In Industry

Revolutionize Clinical Workflows through E-signatures   Clinical trials in India have gained significant importance in the global healthcare landscape. As the nation becomes a hub for clinical research, adhering to stringent documentation processes is crucial in protecting participants and the credibility of research findings. The Government of India has made efforts to introduce guidelines to encourage electronic governance (eGovernance). As India embarks on a journey to a digital economy, it requires innovative solutions to pave its way to success. Clinical researchers are pivotal in finding solutions to burning questions in the healthcare industry. In this blog, we will explore the digitization of documentation, the need to comply with the latest regulations to protect patients, and obtaining informed consent across different types of clinical trials through  electronic signatures in the healthcare industry . Documentation Process in Clinical Trials in India Regulatory Appr...