Our Associate Director, Dr Graeme Deuchar, will be presenting an “Overview and Real World Experience of MHRA’s PIM Designation / Early Access to Medicines Scheme” at the next TOPRA in Scotland meeting. The meeting will be held on 27 September
Orphan Drugs Pricing and Sustainability At a workshop entitled “Sustainable Funding and Fair Pricing for Orphan Drugs: What Are the Solutions?”, the panellists discussed the options that exist to make funding of valuable orphan medicinal products (OMPs) sustainable for healthcare systems while also
By sonia ziouani ammor In Events Tagged Adaptive Pathways, Clinical Trials, Drug Development, Early Access, Early dialogue, EMA, Europe, MHRA, Patient Access, PIM, PRIME, regulatory affairs
With the increasing acknowledgement of the need to develop an overarching scheme to enhance support for sponsors developing medicines, tackling unmet medical needs to ensure timely access to beneficial therapies, the EMA launched the PRIME scheme in March 2016. This
Join top regulators, clinical, safety, and research professionals in health care and drug development. Discuss the biggest challenges, gain new, invaluable insights, and leave inspired to take action. The DIA EuroMeeting goal is to bring together key healthcare stakeholder
By sonia ziouani ammor In Events Tagged Adcetris, ALXN1210, ASH, CAR-T cell, Clinical Trials, Crizanlizumab, CTL019, Glasdegib, Hematology, Highlights, IASLC, Ibrutinib, KTE-C19, Lenalidomide, Obinutuzumab, Oncology, SABCS, WCLC
ASH 2016 Highlights, December 3-6 2016AbbVie Inc. & Janssen – Ibrutinib (IMBRUVICA®). PCYC-1121-CA Phase II trial assessed ibrutinib as a single-agent treatment for marginal zone lymphoma patients that received one or more prior therapies including at least one CD20-directed regimen. In the study, 79% of
