Consultancy

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:

Consultancy Service

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.

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Our Services

Our success, echoed by our clients

Our clients share their experiences of transformation and growth. Unfiltered feedback and the true testament to our service quality.

Their biostatistics and data management expertise streamlined our trial process and helped us achieve submissions on time without any hurdles.

Rajesh Iyer

Clinical Research Director

We relied on their medical writing team for regulatory submissions. The clarity and precision of documents exceeded our expectations

Neha Reddy

Project Lead – Clinical Research

The professionalism and dedication of the team made collaboration seamless. We consider them a long-term partner for future studies.

Dr. Ananya Mehta

Clinical Research Director