DCAT preview: the future of pharma manufacturing

By Kevin Robinson | Published: 10-Mar-2025

Ahead of the upcoming trade show, Dr Kevin Robinson caught up with pharmaceutical industry experts to discuss how they’re innovating for resilience and sustainability in 2025 and beyond

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Thierry Van Nieuwenhove, CEO of Quotient Sciences recognises that sustainability and resilience are critical to the future of pharmaceutical development supply chains.

DCAT preview: the future of pharma manufacturing

As an industry, we must balance the need for innovation and speed with responsible environmental stewardship.

Our ESG commitments at Quotient are deeply embedded in our mission to accelerate the development of new medicines while minimising our environmental impact.

A key example of this is our flagship drug development platform, Translational Pharmaceutics, which integrates formulation development, on-demand GMP manufacturing and clinical testing.

This streamlined approach accelerates drug development while significantly reducing the amount of active pharmaceutical ingredient (API) required.

By minimising material waste and energy consumption, Translational Pharmaceutics helps to lower the environmental footprint of drug development.

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