Focus on Pharma: Assessing in vitro bioequivalence: Nano drug delivery systems

Live Webinar October 24th, 2019

Developing generic versions of complex drug products presents a number of challenges as a result of the nature of their formulation or their route of delivery. In response to this, regulators, including the US FDA, have released product-specific guidance aimed at advising generics manufacturers on the approaches which may be applied to prove bioequivalence in vitro through the measurement of a complex drug product’s physicochemical properties.

In this webinar, we will consider the regulatory guidance available for nano-drug delivery systems such as liposomes, parenteral emulsions, and iron sucrose complexes. These products are considered complex formulations due to the importance of the drug delivery system’s structure and stability in determining the post-delivery fate of the drug product, along with its bioavailability at the site of action. Product-specific guidance documents from the US FDA, along with general guidance from the EMA and Japanese regulators, highlight the importance of physicochemical properties such as particle size and particle charge, along with the formulation structure, phase behavior, and rheology, in assessing drug product bioequivalence. We will consider how this guidance can be followed and will also consider the additional insight which can be obtained through the application of physicochemical analysis techniques in order to aid prototype formulation development and optimization.

Who should attend?

- Researchers considering the requirements for the deformulation of a reference listed drug product

- Formulation scientists engaged in developing candidate generic drug product formulations

- Analytical scientists engaged in supporting in vitro bioequivalence studies

- Laboratory managers looking to understand the techniques required to support deformulation and in vitro bioequivalence assessments

What will you learn?

- The physicochemical properties which are currently highlighted as important for in vitro bioequivalence studies for nano-drug delivery systems

- What Q3 microstructural equivalence is, and how this is important in showing bioequivalence in vitro

- The range of analytical measurement methods available from Malvern Panalytical for assessing bioequivalence in vitro for nano-drug delivery systems

- How techniques such as DLS, NTA, ELS, SEC and SAXS, and rheological analysis can aid formulation development and bioequivalence assessments

You can register for free to all our webinars and you will automatically receive the On Demand version