
Stephanie Sutton
Editor at The Medicine Maker
Articles
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Jan 4, 2024 |
themedicinemaker.com | Stephanie Sutton
Nominations for our 2024 Power List will be closing shortly – specifically on Friday January 12, 2024. This is your last chance to have your say on who will be considered for inclusion in the 2024 list, to be published in April. What is the Power List?
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Dec 27, 2023 |
themedicinemaker.com | Stephanie Sutton
Many industry stakeholders have pointed to a talent shortage in drug development and manufacturing, particularly when it comes to cell and gene therapies. In 2019, a report from the UK’s Cell and Gene Therapy Catapult showed that there were clear concerns in recruiting talent – a problem which persists to this day. In every country hoping to grow its cell and gene sector, recruiting skilled talent is a prerequisite.
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Dec 21, 2023 |
themedicinemaker.com | Stephanie Sutton
In a vaccine production facility, no one can hear you scream. (OK, they probably can but where else can we use such an iconic sci-fi movie reference?). Influenza was a key theme in this issue, with experts exploring why the virus is seen as a “moving target” and how new breakthroughs in vaccines and vaccine manufacturing technology could help. We also report on a visit to the UK’s largest flu vaccine facilities.
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Nov 27, 2023 |
themedicinemaker.com | Stephanie Sutton
The WHO declared the COVID-19 pandemic officially over in May 2023, but the disease continues to make media headlines. In the UK, for example, an outbreak of COVID-19 caused severe flight cancellations in late September at the country’s second biggest airport. In the US, cases are expected to rise over winter, which has triggered the government to re-introduce free at-home testing. Meanwhile, the EU is reportedly talking with Moderna about a new supply deal because of concerns over rising cases.
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Nov 23, 2023 |
themedicinemaker.com | Stephanie Sutton
Last week, the UK’s MHRA conditionally approved the world’s first CRISPR-Cas9 therapy: Casgevy for sickle cell disease and transfusion dependent beta thalassemia. The therapy has been developed by Vertex and CRISPR Therapeutics. A decision in the US is not expected until December 8. It’s a remarkable moment for the CRISPR field – and for patients. “Sickle cell disorder is a very complex life-limiting and life-threatening disorder with very limited treatment options.
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