Thursday, October 15, 2020
In this roundtable you’ll learn about challenges faced by pharmaceutical quality teams in their material analysis workflows, and real-world solutions, how leading pharmaceutical manufacturers have ...
Tuesday, October 13, 2020
In this webinar, you will learn more about current regulatory requirements for residual host DNA clearance for biological products and what that means for gene therapy applications, a demonstration of...
Tuesday, October 06, 2020
In this webinar you'll learn about determining acceptance criteria, what compounds can and cannot be analyzed using TOC, why recovery studies are important and how they are conducted, and the ...
Thursday, October 01, 2020
In this webinar you’ll learn how to understand and characterize ASD physical stability, what the most suitable techniques are for ASD characterization, and linking processability and physical ...
Thursday, September 17, 2020
In this webinar you’ll learn about the improvements made to reduce the chance of cross contamination, improvements made to assist with traceability, and improvements made to assist with the transfer ...
Tuesday, September 15, 2020
In this webinar you'll learn about regulatory requirements for GMP ancillary materials for cell and gene therapy, closed-system manufacturing and how it can improve overall productivity and product ...
Friday, September 11, 2020
This webinar will provide scientists and technical stakeholders working in drug delivery with a detailed explanation of theory and application of an exciting extended release technology platform for ...
Thursday, September 03, 2020
In this webinar you’ll learn formulation screening strategies for amorphous solid dispersions, details on an integrated approach for developing ASDs including performance, stability and manufacture, ...
Thursday, August 27, 2020
In this webinar you’ll learn about how this “lab in a pouch” technology works, primary validation data, and biopharmaceutical company evaluation data.
Wednesday, August 05, 2020
In this webinar, we will explore the use of new technologies and some advanced DSC techniques of the analysis of pharmaceutical materials to better understand how to collect the necessary information ...
This webinar will also focus on how to evaluate this revolutionary technology. From comparability of analytical results across platforms to data integrity and validation testing, this webinar will ...
In this webinar, you'll learn more about regulatory requirements, lot release, in-process testing, risk mitigation, live mycoplasma requirements, sensitivity, specificity, validation considerations, ...
In this webinar, you’ll learn how to accelerate development of SDD formulations, importance of integrated formulation/process development, and mitigate risks during SDD scale-up/development.
In this webinar, you'll learn the risks of omission, inexact identification, and inaccurate and imprecise quantitation in chromatographic screening processes.
In this webinar, you'll learn the components of a method validation per ICH Q2(R1) in the context of a quantitative polymerase chain reaction (PCR) assay for sensitive, accurate and rapid quantitation...