Pavankumar Attuluri

Background

About Pavankumar Attuluri

With over 9 years of experience in regulatory affairs, I focus on facilitating global regulatory submissions at Freyr Solutions. My expertise includes managing US IND, NDA, BLA, DMF, ANDA applications, Health Canada REP processes, EU submissions (DCP, CP, MRP, NP), and Australian NeeS and eCTD submissions. I contribute to original applications, CMC, annual reports, promotional labeling, and safety reports, ensuring compliance with global regulatory standards. At Freyr Solutions, I play a crucial role in planning, preparing, and reviewing regulatory submissions, utilizing my skills in regulatory affairs and document preparation. I am committed to delivering high-quality, compliant submissions that support the efficient lifecycle management of drug products, benefiting both clients and the healthcare sector.