Cervical cancer screening numbers have declined for the fourth consecutive year, according to new figures released by NHS Digital.
Cervical cancer screening numbers have declined for the fourth consecutive year, according to new figures released by NHS Digital.
GE Healthcare has announced the opening of a biotechnology manufacturing centre at the Stevenage Bioscience Catalyst (SBC) Open Innovation Campus, in Stevenage, UK.
Fight for Sight has announced funding for vital research that could help save the sight of children with retinoblastoma.
GP access to appropriate diagnostic tests in the community is currently amongst the lowest in Europe, a report by The Health Foundation has found.
A report published by The King’s Fund has found that improvements in life expectancy have “ground to a halt”.
Takeda’s Alunbrig has been approved in Europe as a treatment for a specific group of lung cancer patients, but access to the drug in the UK remains uncertain.
Bayer and Loxo Oncology’s Vitrakvi has become the first ever TRK inhibitor to be approved in the US, having been cleared to treat advanced solid tumours harbouring an NTRK gene fusion.
The first children to receive Novartis’ Kymriah – a ‘game-changing’ CAR-T therapy for cancer – will start treatment at Great Ormond Street Hospital in London this week, NHS England has announced.
The first edition of the PharmaTimes Medical & Scientific Excellence Awards will take place on Thursday 6th December – the competition will take place during the day, with the dinner and awards ceremony following in the evening at The Sofitel Hotel, Gatwick.
US regulators have granted AstraZeneca’s Fasenra Orphan Drug Designation for the treatment of Eosinophilic Granulomatosis with Polyangiitis (EGPA), a rare and potentially fatal autoimmune disease.
Kyowa Hakko Kirin (Kyowa Kirin) has received marketing authorisation Europe for use of Poteligeo to treat Mycosis Fungoides and Sézary Syndrome.
The Royal College of General Practitioners’ governing Council has passed a motion in support of a second referendum – commonly known as a ‘People’s Vote’ – on Brexit negotiations.
The NHS is set to save a record £300 million after negotiating deals with five manufacturers on low-cost versions of the health service’s most costly drug.
The Mundipharma network of independent associated companies says European regulators have approved use of Pelmeg, a biosimilar of Amgen’s white blood cell booster Neulasta.
Vectura says it no longer plans to develop and partner experimental asthma therapy VR475, after it failed to hit Phase III targets.