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March 16, 2026

Our 2024/2025 ESG report marks a year of progress

We are pleased to announce the release of our ESG report for 2024/2025, which describes our collective progress across environmental sustainability, social responsibility and ethical governance.

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World Orphan Drugs Congress: patient-centricity in practice

Oxford PharmaGenesis recently attended the 6th European World Orphan Drug Congress (WODC) in Geneva, where we observed patient-centricity in action. ‘Patient-centricity’ is a term that is used increasingly to describe organizations’ willingness to put patients at the heart of the treatment development process.

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Oxford PharmaGenesis receives life-saving CPR training

Oxford PharmaGenesis is pleased to be supporting cardiopulmonary resuscitation (CPR) initiatives by providing employees with training opportunities so that they are better equipped to help someone if they are having a cardiac arrest.

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Oxford PharmaGenesis at the World Orphan Drug Congress Europe 2015

So far at the World Orphan Drug Congress Europe 2015, we have been treated to a whirlwind introduction to some of the successes and challenges in the field of rare and orphan diseases.

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Best foot forward to raise funds for rare disease research

Our Managing Director, Chris Winchester, walked 115 km along the Ridgeway this weekend to raise money for rare disease research. He and schoolfriend Justin Brooker set off from Princes Risborough at 7:30 on Saturday morning, and arrived in Avebury 60 hours later bruised and battered but happy.

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Oxford PharmaGenesis at ECTRIMS 2015: HealthScience in action

Oxford PharmaGenesis showcased a broad range of HealthScience services throughout the ECTRIMS (European Committee for Treatment and Research in Multiple Sclerosis) meeting, held 7–10 October in Barcelona, Spain. ECTRIMS is the world’s largest annual international conference devoted to basic and clinical research in multiple sclerosis (MS), with this year’s edition attended by more than 9000…

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Oxford PharmaGenesis release balloons to raise awareness of Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is a progressive and ultimately fatal genetic muscle wasting disease that affects approximately 1 in 3500 newborn boys.1 A fault in the dystrophin gene prevents the production of the protein dystrophin, which is important for muscle structure and function.

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