Phase II and III Clinical Trials

The Context
Your pilot studies deserve the right support in order to ensure the data produced are of the quality and accuracy demanded by competent authorities. Once  the go/ no-go decision has been made to move forward, the focus is on successfully executing  your clinical development program with the ultimate goal of improving quality of care and preventative medicine.

Our Solution
We establish from the beginning what your requirements are and agree a framework for the project including planning, tracking, reporting, escalation and problem solving. Throughout the project our relationship with you and our methods of working are based on our core values and beliefs.
By taking this approach you can be sure that any research we undertake for you will be carried out to the highest possible professional standards.

Our Capabilities
Project Management / Medical Writing
Site Identification and Qualification
Regulatory Affairs / Clinical Monitoring / Medical Monitoring
Data Management and Biostatistics
Pharmacovigilance / Quality Assurance

Call us to find out how our Phase II and III Clinical Trials Solutions can work for you

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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