Biopharmaceutical Analysis

Webinar Date/Time: Wed, Dec 14, 2022 11:00 AM EST

Webinar Date/Time: Friday, December 9th, 2022 at 11am EST|8am PST|4pm GMT|5pm CET

A novel mathematical approach for fitting concentration-response curves is proposed that offers a more accurate estimation of potency data.

Webinar Date/Time: Thu, Dec 1, 2022 11:00 AM EST

Tuesday, November 15th 2022 Morning Session: 11am EST|8am PST|4pm GMT|5pm CET Afternoon Session: 2pm EST|11am PST|7pm GMT|8pm CET Analyzing oligos? Join us to learn about novel, automated, and integrated software to support the analysis of the CQAs of oligos using LC–HRAM MS. Purity and sequencing data will be presented for a multitude of oligos including antisense, aptamer, and long synthetic samples.

The collaboration will see Shimadzu and UMG develop new clinical laboratory methods using LC-MS for TDM analysis.

An orthogonal approach to lipid nanoparticle analysis is recommended to optimize drug development success.

Under this deal, Merck, known as MSD outside of the United States and Canada, will select Veeva products for industry-specific software and data.

A thorough knowledge of both the upstream and downstream processes is required to ensure effective removal of residual impurities in biopharmaceuticals.

Content is king in publishing, but interpretation is imperator.

Using a predictive modeling approach can help tighten up operator control over bioprocessing, which in turn can increase bioreactor output.

OGT has launched the SureSeq Myeloid Plus panel and OGT Universal NGS Complete Workflow.

Using a minimum valuable product and process approach would make it is possible to discipline and structure the development of biopharmaceuticals in the fastest way possible.

Assessment of peripheral blood protein glycosylation has recently become scalable, providing a new domain for biomarker research.

PerkinElmer has unveiled a cell analysis solution to streamline cell and gene therapy research and manufacturing.

A combination of eye imaging techniques and adaptive optics has revealed key details of choroideremia.

The dedicated solid-state research and development suite is designed to promote discovery of novel polymorph, salt, and cocrystal forms.

Using an orthogonal approach to lipid nanoparticle analysis can increase the odds of project success.

A thorough understanding of both regulatory requirements and study challenges can help develop and validate the appropriate methods for a bioanalytical study program.

An early drug candidate screening strategy should incorporate clear targets to lessen late-stage failure.

Avance Clinical’s acquisition of C3 Research Associates expands its CRO services to North America.

Roche’s Digital LightCycler System is designed to aid in diagnostics for cancer, genetic disease, and infection.

A holistic view of the product, manufacturing, and ultimate use of the viral vector is required.

It is important to understand regulatory requirements and study challenges to develop and validate the appropriate methods for a bioanalytical study program at the clinical stage.

CYTENA’s B.SIGHT cell dispenser is designed to streamline single-cell isolation in microbiology research.

The Faustovirus Capping Enzyme launched by New England Biolabs is designed to increase capping efficiency and scalability of mRNA manufacturing workflows.

Guest contributor B.S. Sathya Durga discusses the importance of modernizing India's pharmaceutical manufacturing industry.

Preclinical testing is better able to evaluate complex drug candidates thanks to innovations in animal model approaches.

Synthego has launched new engineered cell libraries to validate targets for quicker drug discovery timelines.

A strong digital backbone is foundational in driving innovation.