Complimenting the broad array of specialised clinical trial services, Cerafor can provide niche biometrics services and consultancy either to bolster clients’ internal resources or as a stand-alone service. Areas of expertise include:
- Medrio database design and deployment
- Production of integrated summaries of safety and efficacy for global regulatory submissions (to CDISC standards)
- Production of CDISC standards and associated documentation
- Mapping of legacy clinical trial data to CDISC standards
- 'Rescue' of studies where prior CRO performance has been inadequate
- Centralised Monitoring
- Providing ‘rapid response’ services to support global submission teams
The above are a flavor of the type of projects that Cerafor can help with. Please get in touch to discuss your specific needs in greater depth.