Magazine: Big biopharma take on the ADC challenge
Antibody‑drug conjugates (ADCs) remain an area of extreme focus in the pharmaceuticals space, with the market projected to hit a…
All articles by Ross Law
Ross Law
Ross Henry Law is a reporter for Medical Device Network. His key interest areas in healthcare include regulation, mental health, neurology, oncology, and Alzheimer's disease. Ross also has extensive prior experience in covering the captive insurance, retail, and technology sectors.
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Accelerating diagnosis and drug development with better managed datasets
Every aspect of science and research is based on data, and across the globe, labs are producing more data than…
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A new way forward in ovarian cancer: why synthetic iMSCs could change the paradigm
Ovarian cancer is one of the most challenging malignancies in oncology. Despite advances in diagnosis and treatment, it is still…
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EpiPen patent expiry opens new era for innovation
The upcoming EpiPen patent expiration on 11 September 2025 sets the stage for a pivotal shift in the epinephrine delivery…
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UK-India $4.8bn FTA poised to benefit medtech and pharma
The UK and India’s newly signed £4.8bn ($6.45bn) free trade agreement (FTA) is expected to give rise to new opportunities…
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Life sciences VC Omega Funds closes $647m funding round
Life sciences venture capital (VC) company Omega Funds has closed its eighth fund, with capital commitments totalling $647m. As with…
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MHRA approves needle-free adrenaline nasal spray for anaphylaxis
The UK Medicines and Healthcare products Regulatory Agency (MHRA) has granted approval for EURneffy, an adrenaline (epinephrine) nasal spray for…
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CTO East Coast 2025: Global oncology cell therapy market to hit $25bn by 2031
According to GlobalData analysis, currently marketed and pipeline cell therapy assets in oncology will generate sales of around $25bn by…
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CTO East Coast 2025: AI can speed up all parts of clinical trial ecosystem
Artificial intelligence (AI) should soon be taking a greater role in areas including patient recruitment and in building efficiencies around…
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CTO East Coast 2025: Navigating shifting regulatory environment hinges on close alignment
With the US Food and Drug Administration (FDA) shifting its clinical trial regulations in recent years, working closely with regulators…