معرفی
Monica Escobar, Ph.D., is a Part-Time Assistant Professor in the Int'l Biomedical Regulatory Sciences and Clinical Trials Programs at the University of Georgia's College of Pharmacy. She holds a Ph.D. in Analytical Chemistry from the University of Florida. With 25 years of pharmaceutical experience, Dr. Escobar specializes in Chemistry, Manufacturing, and Controls (CMC) within Regulatory Affairs, supporting drug development and regulatory submissions globally. She has extensive expertise in oral solid dosage forms, semi-solids, transdermal patches, and liquid parenterals.
Education:
- Ph.D. in Analytical Chemistry, University of Florida
Research Focus: Dr. Escobar's work centers on regulatory compliance, CMC documentation for FDA and EMA submissions, and drug development lifecycle management. She emphasizes practical applications of regulatory standards in pharmaceutical product development.
Teaching & Expertise: She focuses on CMC education, bridging academic training with industry regulatory practices. Her professional experience spans both R&D and regulatory affairs, providing students with real-world insights into global drug approval processes.
Grants & Collaborations: No specific grants mentioned, but her industry experience indicates potential collaborations with pharmaceutical companies on regulatory strategy.
Labs/Teams: Affiliated with the College of Pharmacy's regulatory sciences programs, contributing to interdisciplinary teams addressing biomedical regulatory challenges.
