Advancing single-cell transcriptomics into the mainstream of biomedical research
Kelly Parliament, staff application scientist at Beckman Coulter Life Sciences, discusses how automation is improving the efficiency of single-cell transcriptomic…
Kelly Parliament, staff application scientist at Beckman Coulter Life Sciences, discusses how automation is improving the efficiency of single-cell transcriptomic…
Ryan Rotar, vice president of healthcare market strategy at Tecsys, outlines how supply chain resilience can be maintained in the face of tariffs. Ryan Rotar, vice president of healthcare market…
Regulatory expectations in the drug safety industry have evolved faster in the past five years than in the previous two decades combined. The US Food and Drug Administration (FDA), the…
Dr Karsten Eastman, CEO, Sethera Therapeutics, highlights the challenges around ‘true’ diversification in DNA libraries. In drug discovery, big numbers for screening campaigns are loved. Trillions of molecules! 1020‑member libraries!…
Dr Tommy Rhee, CEO of RheeGen, outlines how FDA crackdowns have revealed dangerous and unethical tissue sourcing practices: Two decades ago, regenerative medicine started out with an extraordinary scientific promise.…
When US Food and Drug Administration (FDA) inspectors arrived unannounced at Hetero Labs' warehouse facility in Visakhapatnam, India, on 19 September , they documented conditions that would result in a…
The pharmaceutical services industry is undergoing both innovation and consolidation – trends that are redefining competition and opening new strategic fronts for clinical technology vendors and contract research organizations (CROs).…