Rao Kasarla

I am having good experience and sound knowledge of Formulation Development with Quality by Design, DOE, FMEA, and Quality Risk Management. Rich work experience in Project management, Budgeting for new products , Pre-formulation Studies, Formulation Development, Process development, Bio-Equivalence Studies, Process Validation, Technology Transfer and with effective communication techniques playing a vital role in creating more productive environment.

Expertised working areas:
1: Solid orals: (Tablet, Capsule and pellets)
2: Semi solids & Liquids
3: Injections (Liquid & Lyophilization)
4: Liquids (Syrups, Suspensions, Gels)
5: Validation, technology transfer and Commercialization
6: Clinical & Bio equivalence (Product development & protocol design)

Experience in regulated environments USFDA, MHRA, TGA and Semi Regulatory.

I have practical proved Expertised skills of Technical, Project management, QbD & PAT technologies.