Pharmaceutical Technology

FEBRUARY 3, 2023

“For each production process, you have to generate the plasmids in huge quantities with GMP quality and then do a transient transfection, meaning you mix them with a transfection reagent and add that to the cells in a very controlled way,” explains Faust. Cytiva and the Drop logo are trademarks of Life Sciences IP Holdings Corp.

Genomics 244

Genomics Genome Medicine Gene Therapy 244

XTalks

JANUARY 6, 2025

Biomanufacturing and Automation The production of vaccines, drugs and diagnostic reagents increasingly depends on good manufacturing practice (GMP) facilities for the manufacturing of critical reagents, a reliance that has intensified since the pandemic. percent from 2021 to 2031, reaching an estimated value of $85.2 billion by 2031.

Gene Therapy 111

Gene Therapy RNA Gene Editing Gene 111

XTalks

MARCH 11, 2025

While RT-PCR methods can handle some level of multiplexing, they do require specialized, contamination-free environments. The result was a prepackaged, off-the-shelf reagent kit that provided reliable quantification for a wide variety of influenza mRNA vaccine constructs.

Vaccination 64

Vaccination Vaccine Development Manufacturing 64