Expert guidance on designing and executing in vitro feeding tube studies,
aligned with USFDA and global regulatory expectations.
Global Consulting Services
TPISTOS provides specialized consulting services to support in vitro study design, execution, and
regulatory alignment. Our expertise spans USFDA expectations, protocol drafting, study method
development, and documentation strategy for successful regulatory submissions.
We assist sponsors, CROs, and R&D teams in navigating technical challenges related to feeding tube
compatibility studies, dosage form preparation, administration techniques, and simulation protocols.
Our consulting scope also covers IVRT/IVPT for topical formulations and BCS-based biowaiver
studies, ensuring data integrity and regulatory acceptance.
With a deep understanding of global compliance standards and study-specific nuances, TPISTOS
empowers you to streamline development and meet submission timelines with confidence.
Feeding Tube Study
IVRT/IVPT Study
Consulting support for in vitro permeation and release testing of
topical formulations, ensuring scientifically
robust and regulatory-compliant study design.