Arti Jinsi-Parimoo Regeneron
Arti Jinsi-Parimoo Regeneron Director, CMC Regulatory Affairs
Dr. Arti Jinsi-Parimoo has expertise in manufacturing and regulatory development of pharmaceuticals and medical devices through various stages of clinical development to global commercial path. Led and managed projects to meet time-cost objective with high quality results. Performance-driven scientist adept in innovative management practices that drive business growth via collaborations. Expanded skill expertise in clinical and regulatory drug/device development through certification and hands-on practice. She is also a NJ Registered and Authorized Nuclear Pharmacist with RAC certification.
Dr. Arti Jinsi-Parimoo specializes in regulatory strategic support for development of small molecules, biologics and medical devices, clinical supply and trials and post-marketing support, Project management, QA and Compliance, technical expertise in development of analytical and bioassays for RNA, DNA and protein analysis, protein purification, cellular analysis, assay design, cell culture & animal models, chromatographic & fluorescent methods, GPCRs, signal transduction, receptor pharmacology, oncology, inflammation, cardio-vascular markers, diagnostic imaging modalities, six sigma quality.