Developing and manufacturing innovative pharmaceutical products requires a partner who understands the complexities of bringing new chemical entities, biologics and live biotherapeutics to market. Our custom-designed clinical trial, commercial manufacturing and packaging solutions meet the unique needs of your project. As an agile UK-based Contract Development and Manufacturing Organization (CDMO), we provide flexible GMP manufacturing, supporting projects from FIH trials through to phase III clinical supplies manufacturing. Whether you need non-GMP feasibility studies or phase-appropriate cGMP Clinical Trial Material (CTM) production, we have the expertise to help you succeed.
Benefit from comprehensive clinical trial, commercial manufacturing and packaging solutions
- Achieve clinical trial and commercial success
We offer comprehensive support from non-GMP feasibility studies to phase-appropriate cGMP manufacturing, ensuring your project progresses smoothly from development to commercialization.
- Benefit from flexible manufacturing solutions
Our UK-based CDMO provides agile and adaptable GMP manufacturing services, tailored to meet your specific project requirements from FIH through to phase III clinical supplies.
- Leverage proven manufacturing technologies
Our extensive experience and use of proven technologies reduce economic risks, enabling rapid entry into FIH trials and accelerated scale-up for future clinical phases.
- Access a wide range of manufacturing and packaging capabilities
We offer a broad spectrum of clinical trial manufacturing and packaging services, including oral liquid manufacturing, granulation, blending, tableting, capsule filling, banding, coating and more.
Why SGS?
As a global leader in inspection, certification and testing, we provide unparalleled expertise in the development and manufacturing of pharmaceutical products. With over 250 successful projects delivered, our team of technical experts brings in-depth knowledge and experience in formulating and analyzing new chemical entities, biologics and live biotherapeutics. We are committed to continually developing pharmaceutical products with world-leading expertise that ensures safety, quality and commercial viability. Our agile approach allows us to tailor services to your specific needs, providing low-risk, high-quality solutions that accelerate your journey from development to market.