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GMP
GMP is an acronym used in two instances: Guanine Monophosphate ( a biomolecular consisting of a phosphate group, pentose sugar ribose, and guanine base), and Good Manufacturing Practice (the system used to ensure the high quality manufactured products).
OCT 15, 2025 | 2:30 PM
Cell isolation and activation are critical for cell therapy development and manufacturing. Ease of use, regulatory compliant and financial sustainability are among the most important conside...
OCT 15, 2025 | 5:30 AM
In recent years, non-viral methods for cell engineering have emerged as promising alternatives to viral transduction. Amongst the virus-free technologies, electroporation is considered the g...
OCT 07, 2025 | 11:00 AM
Mass Photometry (MP) and Macro Mass Photometry (MMP) are complementary, label-free techniques that analyze biomolecules and therapeutic vectors directly in solution with single-particle reso...
MAR 25, 2025 | 8:00 AM
Analytical ultracentrifugation is an established method during the development of therapeutic proteins and antibodies and contributes supporting information regarding the size, oligomerizati...
MAR 12, 2025 | 8:00 AM
For large-scale enrichment and isolation of immune cells or stem cells for cell therapy applications, common cell purification platforms separate cells based on a single surface antigen. Enr...
MAY 29, 2024 | 8:00 AM
A-TEEM spectroscopy is an emerging technique with huge potential for QC laboratories in the pharmaceutical and biopharmaceutical industries. We present a set of tools for A-TEEM spectroscopy...
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C.E. CREDITS
Hop latent viroid (HLVd) infection lowers the commercial value of cannabis by reducing flower harvest weight, THC concentration, and terpene production. Unlike other microbial contaminants i...
APRIL 12, 2024 3:30 PM ET
As you transition your discovery through research and development to commercial production in a GMP setting, your goal is to speed that process by minimizing variables. Laboratory equipment...
APR 03, 2024 | 6:00 AM
Quantifying critical quality attributes accurately and precisely is an important aspect of regulatory compliance. There is greater demand to optimize processes by integrating advanced analyt...
MAR 20, 2024 | 1:00 PM
As workflow efficiency and data reproducibility are common challenges faced by scientists for high throughput laboratories, GenScript has developed unique automation technologies to address...
On Demand
C.E. CREDITS
Validation of computerised systems is a regulatory requirement for both GMP and GLP laboratories. Although computerised system validation (CSV) has been required for over 40 years, the appro...
DEC 05, 2023 | 8:00 AM
CGX10 Cell Isolation System: Introduction, Utility, and Assessment in a GMP-grade Environment for Multiparametric Cell Sorting A future of long-term, minimally toxic immunotherapy personaliz...
NOV 01, 2023 | 10:30 AM
With the fast progress and deeper understanding of CAR-T cell therapy, finding a better solution other than lentivirus transduction is more requested, to overcome the functional limitation o...
