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              Bioconvergence: Future trends for biomedicine

              Dr. Tom Knapman, Director of Strategic Brand at SCIEX, explains how bioconvergent advances will help [...]

              Lab of the future: an expert view

              The Lab of the Future will fuse automation, speed and remote work says Thomas Marshall, [...]

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        Listicle

        Listicle: Driving production in biologics with automation 

        4 May 2022

        Drug development technology has evolved rapidly in recent years, and with the industry advancement comes an increased capability of producing high-quality targeted large molecule drugs such as biologics and biosimilars. The significance of biologics is far-reaching, including treatment of rheumatologic diseases, cancer, diabetes and anaemia. The range of therapy modalities is ever-expanding and at present […]

        Listicle: Lithuania’s biotechnology growth strategy

        3 March 2022

        Lithuania is dedicating time and resources establishing itself as a life science and biotechnology hub of excellence. DDW’s Megan Thomas analyses four pillars of Lithuania’s growth strategy, which involves ensuring female scientists take leading roles in industry, focusing on investment, developing a strong talent pool as well establishing itself as a go-to destination for clinical trials. […]

        Listicle: Experts on the differences between FDA and EMA regulations

        6 October 2021

        Biotechs involved in drug discovery have to navigate increasingly complex regulatory environments across borders. Experienced experts and non-executive advisors to Arriello, Eric Caugant, Principal Consultant at Pharmacovigilance Systems Consulting & Board advisor to Arriello, and Judi Sills, JM Sills Consulting & Board advisor to Arriello, highlight the main differences between US and EU requirements, and advise on […]

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