PHARMACEUTICAL DRUG DEVELOPMENT PROCESS:
Role of Dissolution Testing
This Professional Development Certificate Course Series on the Role of Dissolution Testing in Pharmaceutical Drug Development provides a comprehensive mass of critical information to the R&D (formulation and analytical), QC/QA, Regulatory Affairs and PK professionals concerning the intricacies associated with effective dissolution testing, from basics to advanced applications including correlating dissolution and bio-availability as well as bio-waivers and clinical applications of IVIVC.
This Professional Advancement Course Series comprises six (6) short focused intensive modules structured as building blocks – from basics all the way to bio-waivers and clinical applications. Each course is profuse with numerous examples and case studies as well as the instructor’s vast experience(s) which provide a practical perspective of dissolution testing at various stages in drug development process to the participants. It is anticipated that the judicious combination of theoretical details and practical considerations employed by the instructor(s) will provide a consolidated and holistic understanding of the role of dissolution testing in pharmaceutical drug development process.
- Module I
PHARMACEUTICAL DISSOLUTION TESTING:
Fundamentals and Advanced Applications - Module II
BIOEFFICACY CENTERED DISSOLUTION
METHOD DEVELOPMENT
Applications and Analyses - Module III
DISSOLUTION AND BIOAVAILABILITY
Fundamentals and Applications of IVIVC - Module IV
Automation in Dissolution Testing & Dissolution studies for novel drug delivery systems - Module V
QbD in Dissolution Method Development
QTTP, Critical Method Atributes, Discriminatory Method.DOE s, Method Finalization - Module VI
IVIVC, BIOWAIVERS AND CLINICAL APPLICATIONS OF IVIVC
For inquiry write to contact@spds.in