In Vitro Bioequivalence Studies Of Topical Drug Products: Challenges And Promises Of Ivrt And Ivpt

In Vitro Bioequivalence Studies of Topical Drug Products: Challenges and Promises of IVRT and IVPT

U.S. Food and Drug Administration

In Vitro Bioequivalence Studies of Topical Drug Products Challenges and Promises of In Vitro Release

In Vitro Bioequivalence Testing of Topical Generic Products

Teledyne Hanson Research

2021 IVRT/IVPT Workshop Day 1 Foundation Lecture

Center for Research on Complex Generics (CRCG)

Complex Generics: Topical Products, Part 1

U.S. Food and Drug Administration

IVRT IVPT: A Contemporary Overview of Testing Methods and Regulatory Guidance

In vitro bioequivalence testing for topical ophthalmic suspension products (17of39) Complex Generics

U.S. Food and Drug Administration

A New Possible Way to Evaluate Bioequivalence of Topical Drugs

U.S. Food and Drug Administration

In Vitro Release Testing for Complex Generics: A Bioequivalence Perspective

U.S. Food and Drug Administration

In Vitro and In Vivo BE Approaches: Challenges and Opportunities – Session 3B

U.S. Food and Drug Administration

Developing and Implementing Science-Based Standards in Bioequivalence Assessment

U.S. Food and Drug Administration

Complex Generics: Topical Products, Part 2

U.S. Food and Drug Administration

2021 IVRT/IVPT Workshop Day 1 Dr. Audra Stinchcomb Presentation

Center for Research on Complex Generics (CRCG)

In Vitro Studies for Alternative BE Approaches to Comparative Clinical Endpoint BE Studies

U.S. Food and Drug Administration

2021 IVRT/IVPT Workshop Day 1 Panel 2 Skin Selection, Preparation and Storage

Center for Research on Complex Generics (CRCG)

In Vivo Dermal Microperfusion & Microdialysis Bioequivalence Approaches

U.S. Food and Drug Administration

Topical Dosage Forms: Emerging Insights and Implications for Bioequivalence Approaches

U.S. Food and Drug Administration

Assessment of Complex Drug Product – Physicochemical Characteristics to Support In Vitro BE Studies

U.S. Food and Drug Administration

PBPK to Guide Study Design and Product Development for Generic Dermatological Products

U.S. Food and Drug Administration

Webinar: Introduction to In Vitro Release Testing (IVRT)

Teledyne Hanson Research