In the evolving pharmaceutical industry it is necessary to keep the pace by constantly registering new drugs and opening new markets for the already existing ones.
This process has become more and more complex along time with the participation of multiple departments and personnel inside the pharmaceutical company and Contract Research Organizations (CRO), which in some cases, are located in several countries.
In such scenario, the pharmaceutical company should ensure that all the stakeholders in the project have the appropriate quality system, working in accordance with the Good Clinical Practices.
TDV provides its expertise in GCP projects for:
- Implementation and improving quality system in CROs and medical research departments
- Internal audits in medical departments and audits to CRO
- Audits of clinical & bioequivalence trials
- Validation of Clinical Data Management computerized systems
For further information about Good Clinical Practices, please contact: