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Year: 2018

Holiday CSR Activities

SEKISUI understands that a better future starts with our actions today, and encourages its global family to remain focused on...

FDA Guidance: Many In Vitro DDI Evaluations Should Precede FIH Studies

In October 2017, the FDA released its much-anticipated draft guidance documents for drug-drug interaction (DDI) studies, which was finalized in...

SEKISUI Continues Environmental Awareness

SEKISUI at Natural Capital Week in Paris On Wednesday 28th November, the Natural Capital Coalition: Collaboration Day took place in...

Coverage from the October 2018 PBSS DDI Workshop

The Pharmaceutical and BioScience Society (PBSS) hosted the workshop “Drug-Drug Interactions: Update on Risk Assessment, Clinical Evaluation and Regulatory Requirements” on October...

October Presentations on In Vitro Effects of Biologics on CYP Enzymes and Regulatory DDI Guidances

On Oct. 15th at the Peptide ADME Discussion Group Workshop in Gothenburg, Sweden, Dr. Brian Ogilvie presented on In vitro Direct and Cytokine-Mediated...

To GLP or not to GLP?

That is the question. . . Knowing the answer may save you time and money Good Laboratory Practices (GLP) are...

New Recommendation: Evaluate NMEs for OCT1 Transporter-Mediated DDI Potential

Brian Ogilvie, Ph.D., Vice President of Scientific Consulting at SEKISUI XenoTech, presented a case study on the importance of the hepatic...

Cypex Expands Portfolio of Recombinant Enzymes

As the exclusive distributor for Cypex in the US and Canada, SEKISUI XenoTech is proud to offer this portfolio of products based...

New Rodent, Monkey CryostaX Hepatocytes Featured in Industry News

Following SEKISUI XenoTech’s announcement SEKISUI XenoTech Adds Monkey, Rodent Hepatocytes to Patented CryostaX Product Line, Anticipates the End of Traditionally Cryopreserved...

Challenges & Solutions in Today’s In Vitro Transporter Research

Transporters are membrane-bound proteins that govern the passage of drugs into and out of cells. These gatekeeper proteins can be...

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