Development of a scalable manufacturing process
How GRA assisted in the development of a scalable purification process for a novel live attenuated viral vaccine for First-in-Man trials.
what we do
How can you improve biotech development?
With over 1000 years of collective biopharmaceutical discovery, development and launch, we are experts in what we do. Whether you are in discovery, figuring out formulation, identifying your CDMO or trying to value your product, we help you reach your destination quicker. Click through to our service page to see how we can help, or our case studies to see how we have helped other clients.
But more than this, we also have a number of levers that we use to accelerate the process and bring your team along on the journey. These help maximise budget and condense the time needed during each phase. Click through and see how these can help your organisation:
For more immediate fixes. We can support end-to-end activities across the following service areas:
- CMC and Manufacturing
- Programme and CDMO Management
- Assays and Quality Control
- Formulation Development and Stability
- Quality Assurance and Regulatory
- Preclinical, Nonclinical and Toxicology
- Strategic Planning and Due Diligence
- Clinical Development and Monitoring
Get in touch with GreyRigge.