LCMS webinars focusing on Dissolution | LabRulez LCMS

Solving Problems That Matter - a Waters webinar series featuring USP speakers. Episode 10: Performance Verification Testing in Dissolution

We want to provide you with an overview of how Quality by design (QbD) has evolved and especially what the authorities expect from your dissolution method development.

With the discussions and initiatives around real-time release testing, we want to look at how this topic could influence what dissolution testing looks like in the future.

This overview should help you with your compliance projects and your preparation for the next audit.

What could be a better indicator to assure the quality of the generic product than dissolution testing? Join the meeting and make this an interesting discussion with your questions and insights.

The discussion will highlight some advantages and disadvantages of PQ and MQ approaches and give you some insights on which approach could work best for your lab.

Release profile of poly (lactic co-glycolic) (PLGA) nanocapsules loaded with all-trans retinoic acid (RA). Dissolution Studies with NanoDis

Release-rate testing basics and method development considerations for cannabis-related products.

Key aspects of the dissolution workflow that can be accelerated to produce data faster and reduce overall time between tests.

Do you wish to quickly uncover the best nanoparticle formulation, and achieve accurate and reliable results in any dissolution tests for tablets or liposome drug products?