Newsletter | July 22, 2025

07.22.25 -- FDA Leading The Decline Of Animal Testing

FEATURED EDITORIAL

FDA Leading The Decline Of Animal Testing

The gold standard practice of conducting animal studies for evaluating toxicity, pharmacodynamics, and immunogenicity is being challenged by innovative alternatives – New Approach Methods (NAMs).

Formulation Development Of A JAK1 Inhibitor Extended-Release Tablet

This scientific article presents a summary of the formulation development strategy of a JAK1 inhibitor extended-release tablet, with a focus on experimental design, data interpretation, and formulation decision-making.

INDUSTRY INSIGHTS

Preclinical Studies Of Gene Therapy Products: Latest Trends

Check out this essential webinar, where our experts provide an in-depth review of gene therapy approaches in nonhuman primates.

Application Of A Novel Temperature Shift Process For Particle Engineering

Spray drying of amorphous dispersions improves solubility and bioavailability, enabling supersaturation in the intestine and driving higher absorption rates when compared to crystalline drug forms.

Extractables And Leachables: Risk Management And Analytical Solutions

Partnering with a CDMO that offers comprehensive and robust E&L studies can help facilitate a smooth product launch by ensuring minimal impact from impurities, all while mitigating risks.

Quantification And Qualification Of Adeno-Associated Virus

Discover how digital PCR enables precise, reproducible AAV quantification, overcoming qPCR limits with streamlined workflows and CGT-specific assays for safer gene therapy development.

Quality Control During Membrane Protein Purification For Cryo-EM

Overcome the challenges of membrane protein purification for cryo-EM. Learn essential quality control techniques to ensure your samples are homogenous and suitable for downstream structural analysis.

SOLUTIONS

Solid Form Services

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