Regulatory affairs play a crucial role in safeguarding public health by ensuring the safety, efficacy, and quality of pharmaceutical products. This research article explores the multifaceted responsibilities of regulatory affairs professionals in the drug development process. It examines their role in navigating the complex regulatory landscape, fostering compliance with evolving guidelines, and facilitating communication between various stakeholders. The article also highlights the significance of regulatory affairs in promoting innovation, addressing global harmonization efforts, and fostering public trust in the pharmaceutical industry. Overall, this research emphasizes the critical role regulatory affairs plays in maintaining drug safety and efficacy throughout the product lifecycle.
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Pharmaceutical Regulatory Affairs: Open Access received 533 citations as per Google Scholar report
