Clinical Monitoring

The Context

Our Clinical Research Associates (CRAs) are one of the strongest links in the chain of a clinical study and act as the main line of communication between investigators and our clients. While always ensuring subjects' wellbeing and rights and data reliability, they promote and uphold the image and values of our clients’ company at all times. Their professionalism and enthusiasm is second to none in the market.
We offer our CRAs a comprehensive internal and external training program featuring Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and regulatory requirements. In addition, they receive project specific training before the start of any projects.
All monitoring activities are conducted according to the international standards of ICH/GCP.
With the support of their Project Manager and Line Manager, our CRAs are accountable for:

- Investigational site identification and qualification
- Collection, review and tracking of essential documents
- Site initiation, ongoing monitoring and closure of investigational sites
- Reporting and tracking of monitoring activities
- In-house site management
Our solutions:
 Early Stage Clinical Trials / Phase II and III Clinical Trials
 Late Phase Clinical Trials / Post Marketing Safety Studies
 Product Value and Effectiveness in Real-world
 Public Health and Social Science Research

Why Africa

Africa offers an increasing number of experienced researchers through networks of excellence implemented ...

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Partners

At Pharmalys we believe in the value of partnership, sharing knowledge and establishing synergies in order to develop innovative solutions ...

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Become an Investigator

You can make a difference to a noble cause by getting involved in health related studies

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Contact

Pharmalys Ltd UK
Tel: +44 208 0909 620

Pharmalys SARL Senegal
Tel: +221 33 825 42 43

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