What We Do
We coordinate individual specialist skills, capitalising on their combined value to meet the individual needs of each client.
The multidisciplinary group has wide-ranging experience in toxicology, regulatory science and project management with special focus on:
- Overall strategy, strategic planning and management of the development and registration process
- Dossier preparation and submission for the pharmaceutical and chemical industry and safety assessments for consumer products
- World-wide track record of successful regulatory documentation
- Experienced managers of international, cross-functional teams and consortiums to facilitate data sharing, strategy optimisation, submission and registration
- World-wide successful registration track record of successful regulatory documentation
- Key contacts within the scientific community and regulatory authorities
- Individuals regarded as experts within their specialist fields, with hands-on experience in industry and CROs
- Recognised expertise in Reproduction and JuvenileToxicology, Developmental Neurotoxicology and Immunotoxicty
- GPC have a network of independent associates for wider specialist expertise
- Code of conduct – GPC uphold the principles of scientific authorship and review set down by major scientific societies and is fully independent of any CRO
