• Ambekar Utkarsha Rajendra
• Miss.Kaveri T Vaditke

The pharmaceutical industry stands at the forefront of scientific innovation, dedicated to the development and production of life-saving drugs. At its core lies Regulatory Affairs, a critical function responsible for ensuring that pharmaceutical products meet the stringent requirements set forth by regulatory authorities. In this context, Analytical Development plays a pivotal role, providing the scientific foundation upon which product quality and efficacy are determined. This document explores the multifaceted world of Regulatory Affairs within the pharmaceutical industry, with a specific focus on its intersection with Analytical Development. It delves into the key responsibilities of Regulatory Affairs professionals, emphasizing their role in navigating the intricate web of regulations governing drug development, manufacturing, and quality control. Through case studies and practical insights, we shed light on the strategies employed to secure regulatory approvals and maintain compliance.

Regulatory Affairs, Pharmaceutical Industry, Analytical Development,Regulatory Bodies.

"Regulatory Affairs In Pharmaceutical Industry In Analytical Developement", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.11, Issue 1, page no.f115-f131, January-2024, Available :http://www.jetir.org/papers/JETIR2401516.pdf

"Regulatory Affairs In Pharmaceutical Industry In Analytical Developement", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.11, Issue 1, page no. ppf115-f131, January-2024, Available at : http://www.jetir.org/papers/JETIR2401516.pdf