Labroots is pleased to announce the 7th Annual Event in the 2023 Cannabis Sciences Virtual Event Series . Labroots will host the event on April 17, 2024. The Cannabis Sciences planning commi...
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...
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...
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...
Genetics may influence experience with cannabis and CBD. With increased access to legal cannabis and the research community expanding their focus on the medicinal uses of cannabinoids, more...
The escalating demands for operational efficiency, precision, and regulatory adherence in analytical laboratories necessitate the adoption of advanced technological solutions. Laboratory Inf...
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...
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...
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...
Stago EdVantage Virtual University is an educational platform that demystifies hemostasis testing with on-demand webinars and a virtual exhibit hall that ......
Clinical laboratories often interact their information technology (IT) department, especially when installing new instruments, adding new tests to the menu, defining critical values, analyzi...
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...
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...
Labroots is pleased to announce the 6th Annual Event in the Bioprocessing Virtual Event Series ! Join us for this free, one-day event on April 3, 2024 as we discuss upstream and downstream p...
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...
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...
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...
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...
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...
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...
Effective process development for viral vector-based medicines is paramount for optimized process efficiency, robustness, scalability, and product quality. Well-designed processes streamline...
The implementation of a preemptive pharmacogenomics (PGx) program in a hospital setting requires a multidisciplinary approach to ensure seamless integration of each stage of the process for...
The implementation of a preemptive pharmacogenomics (PGx) program in a hospital setting requires a multidisciplinary approach to ensure seamless integration of each stage of the process for...
Welcome to the 8th Annual Event in the Laboratory Automation Virtual Event Series ; a free virtual conference for professionals interested in the most recent technologies for today’s l...
In the MIT Media Lab global synthetic biology course ‘How To Grow (Almost) Anything,’ students from MIT, Harvard, and a global classroom of hundreds learn concepts and skills at...
Welcome to the Guardians of Science, Ask the Expert Webinar Series! Join our distinguished Thermo Fisher Scientific team of experts as they delve into the topics of advanced technology and pl...
Join us in this enlightening session to deepen your understanding of qualifications and their transformative impact on risk management and regulatory adherence. Gain actionable insights that...
Nanovials are emerging as an accessible platform for performing single-cell functional screening leveraging standard instrumentation, such as flow cytometers and microfluidic single-cell seq...
Embarking on the journey of LIMS data migration, whether it's transitioning to a new LIMS or upgrading to a more advanced version, may initially appear as a straightforward task. However...
Learning Objevtives: 1. Demonstrate Knowledge with gene editing, microfluidics and non-viral delivery methods. 2. Review the uses of a low-volume high-throughput transfection platform for ge...
This talk will focus on doing method validation work in an environment where data is gathered from laboratory information system and chromatography data system. We’ll see how these sys...
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...