Paratus Clinical has an uncompromising focus on maintaining the highest quality standards across all our locations and for all clinical trials. Internal processes and procedures are backed-up by a range of external audits commissioned by trial sponsors and various regulators. We are proud of our exemplary record of quality and welcome any review or audit.
A member of our Quality team will be actively involved in your study from start-up through to completion undertaking the following activities:
- Risk assessment
- Study initiation visits
- First participant review
- Review monitoring follow-up letters
- Host audits
- Escalation of any quality issues
- Close-out visits
Monitoring
We regularly review our Standard Operating Procedures and clinical procedures. Our quality team conducts regular site monitoring visits and works closely with the site managers to implement Corrective and Preventative Action (CAPA) plans.
Consistent internal monitoring is undertaken by the Quality team and includes:
- Investigator Site File (ISF) review
- Internal monitoring after first participant randomised
- Preparation of internal monitoring plan
- Peer-to-peer monitoring
Audits/Inspections
We have an excellent track record and high performance in audits undertaken by a range of third-parties, including:
- Sponsor audits
- HREC audits
- OGTR inspections
- CRO Process audit
- Voluntary Inspection
