Quality Assurance

The Context
We perform audits at all stages and on all processes used in the management of clinical trials and health related studies to assess adherence and compliance with SOPs, GCP, regulatory requirements, study protocols, client instructions and contractual obligations.
Our services include the following types of audit:
- Investigational site facilities
- Study data
- Trial master files and investigator site files
- Monitoring compliance
- Clinical trial documents including clinical trial reports

We can also provide the following ad-hoc services:
- Review of current structure and policies, processes and documentation
- Identification of corrective and preventive actions for process improvement
- Implementation of a comprehensive and efficient system enabling a consistent    quality structure
- Writing, reviewing or updating SOPs

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

- Scientic and Clinical product Support
- Pharmacovigilance

 

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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