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Cannabis edibles and orally administered oils act slowly and unreliably because the incorporated cannabinoids do not dissolve in water. Similar poor performance profiles are observed for oth...
ISO 17025 accreditation ensures laboratories provide high-quality testing services. However, the path to achieving compliance could be riddled with challenges for new and established labs al...
In the rapidly evolving landscape of cannabis production and consumption, ensuring the safety and quality of cannabis products is of paramount importance. Microbial contaminants pose potenti...
The escalating demands for operational efficiency, precision, and regulatory adherence in analytical laboratories necessitate the adoption of advanced technological solutions. Laboratory Inf...
BACKGROUND: Chemotherapy-induced nausea and vomiting (CINV) is a debilitating side effect of cancer treatment, affecting up to 40% of patients. Cannabinoid agonists such as nabilone and &Del...
Effective control of the spread of HIV depends on using the right antiretroviral drugs. In 2019, the World Health Organization recommended using the integrase inhibitor, dolutegravir (DTG), i...
Clinical laboratories often interact their information technology (IT) department, especially when installing new instruments, adding new tests to the menu, defining critical values, analyzi...
The Comprehensive Genomic Profiling (CGP) ctDNA (circulating tumor DNA) panel generates complex biomarkers, e.g., tumor mutational burden and microsatellite stability status along with mutat...
Every area of the laboratory has specific issues with pre-analytical errors causing unreadable or false results on samples, from mislabeling to samples being forgotten on the floors to drawi...
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...
LIAISON(R) MeMed BV(R) is an innovative test based on computational integration of three host immune response proteins, TRAIL, IP-10, and CRP to differentiate bacterial from viral infections...
Leveraging advancements in spatially resolved single-cell profiling, our study enhances understanding of glioma evolution and the complex tumor microenvironment. Through spatially resolved m...
Throughout the journey from manufacturing to patient delivery, low efficiency and poor biocompatibility of conventional preservatives are barriers to successful cell preservation. Our webina...
Cell and gene therapies are on the brink of transforming the pharmaceutical industry, presenting unique challenges such as ensuring the quality and consistent supply of reagents. Reagents pl...
mRNA vaccines represent a pivotal innovation in prophylactic healthcare, offering a rapid response to emerging infectious diseases. Leveraging the cellular machinery to produce antigenic pro...
Human induced pluripotent stem cells (hiPSCs) are a powerful tool for innovative approaches, such as drug discovery, in vitro disease modelling, or regenerative therapies. However, such proc...
We are leading the way in developing integrated online sampling and Process Analytical Technology (PAT) workflows for quick monitoring of critical quality attributes (CQA) to produce advance...
Join this year's poster presenters in the Poster Hall during the Poster Networking Hour, Wednesday, March 6th, from 10:00 AM –11:00 AM PST, to chat live about their posters and lat...
Cultured mammalian cells, particularly Chinese hamster ovary (CHO) cells are widely used in the biotechnology industry for production of a wide range of therapeutics, predominantly monoclona...
Gene therapy has revolutionized the field of medicine, and it has the potential to cure a wide variety of genetic disorders. Gene therapy involves the introduction of a functional gene into...
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...
Nanoparticle mRNA Therapeutics has been the focus of intense research driven by the safety profile and several clinical breakthroughs. As of March 2024, there are two mRNA vaccines approved...
In the slowly evolving landscape of bioprocess development and manufacturing, digital bioprocess-twins have emerged as potential accelerators. While advanced algorithms are at the heart of t...
Efficient utilisation of abundant renewable sugars and aromatic chemicals by natural or recombinant microorganisms is a key prerequisite for the economic viability of biotechnological valori...
Effective process development for viral vector-based medicines is paramount for optimized process efficiency, robustness, scalability, and product quality. Well-designed processes streamline...
Chimeric antigen receptor T-cell (CAR-T) therapies have emerged as a revolutionary approach in the field of hematological malignancies, offering unprecedented clinical efficacy when patients...
Self-removing affinity tags have the potential to greatly accelerate the development of new therapeutics, while providing a potentially enabling manufacturing platform for non-mAb therapeuti...
Cannabis edibles and orally administered oils act slowly and unreliably because the incorporated cannabinoids do not dissolve in water. Similar poor performance profiles are observed for oth...
