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Within the pharmaceutical landscape, drug regulatory affairs stand as an important pillar. Quite frankly, it is defined as the nexus of the convergence of science, law, and patient welfare. An orchestration of processes and protocols makes sure that pharmaceutical products are able to fulfill their purpose well.  Drug regulatory affairs certification  ensures the presence of professionals who can further ensure safer products. This article traces the evolution of drug regulatory affairs throughout the years. Know The Trends In And The History Of Drug Regulatory Affairs Professionals who have done certificate courses in drug regulatory affairs serve as the custodians of public health. They are in charge of looking after the intricacies of rules, protocols, and other standards set by the regulatory authorities. This process has seen a lot of ups and downs since its advent and has a long history of evolution so that pharmaceutical drugs become safer for common use. The primary purpose tha