Date of Award
2019
Document Type
Dissertation
Degree Name
Ph.D. in Pharmaceutical Sciences
Department
Pharmaceutics and Drug Delivery
First Advisor
Soumyajit Majumdar
Second Advisor
Seongbong Jo
Third Advisor
Michael A. Repka
Relational Format
dissertation/thesis
Abstract
Through the process of drug development, a molecule goes through discovery screening; lead selection and optimization, ADME testing, toxicity profiling, dosage form determination, preclinical testing in an in vitro and in vivo setup, folloby clinical research, FDA review and approval until eventually it is manufactured in the determined dosage form and reaches the patient. At every point through this process, scientists actively work towards a smoother transition and a quick and safe approval of the molecule towards the next step. The different chapters in this research would cover various phases of drug development; from discovery stage to fill-finish and primary container compatibility.
Recommended Citation
Taskar, Pranjal, "Formulation Development, Preclinical Testing, and Primary Packaging Optimization for Cannabinoids and Other Therapeutics" (2019). Electronic Theses and Dissertations. 1711.
https://egrove.olemiss.edu/etd/1711