Seda provides integrated Pharmaceutical Development and Clinical Pharmacology services, driving value creation from strategic planning, design, data interpretation, to execution. Our recently added GMP manufacturing capabilities now enable us to deliver an end-to-end service, supporting clients from development through to clinical trials.

Located in Greater Manchester, Seda combines expertise and a proven track record to ensure clients' products are in trusted hands. Our team has successfully developed, submitted, and launched numerous medicines across therapeutic areas, with a particular strength in Oncology, including drugs with 'breakthrough' status. Pioneering innovative approaches to streamline project timelines, Seda creates significant value and cost efficiencies for clients.

Our team of experts brings deep scientific knowledge across a wide spectrum of disciplines and development stages, from discovery through to product launch.

Our Services and areas of specialism Include:

Routes of Administration & Technologies:

Oral: Immediate Release, Modified Release, Oral Poorly Soluble

Parenteral: Standard Injectables, Complex Injectables, Poorly Soluble IV, Depot

Targeted Delivery: Nasal and Inhaled

Other Services:

Pharmacokinetic (PK) Modelling

Technology Transfer

Commercialisation Support

Proprietary, in-house GMP Manufacturing and Analytical Services

CDMO Selection and Due Diligence



With Seda, you gain a trusted partner dedicated to delivering high-quality solutions underpinned by scientific excellence, supporting your journey from concept to clinic with precision and reliability.

Maximising value from asset to approval \