Lonacas Consultants 

Our Clinical Research Team is comprised of highly trained professionals in managing investigator sites with the utmost efficiency and providing clinical monitoring services.

Our clinical monitoring and site management services include:

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• Site Identification and feasibility.

• Review of inclusion, exclusion criteria and the proper consenting of all subjects.

• Site selection and qualification visits.

• Assist with obtaining approval from Local Ethic Committees and Institutional Review Boards.

• Manage subject recruitment.

• Review of quality systems at the site and ensuring all sites are audit ready.

• Initiation, interim monitoring, and study closure visits.

• Essential document collection, review and processing.

• Source documentation review, CRF review and query resolution.

• Accountability for all study documents and materials.

• Communication with Sites.

• Study specific training to site personnel.

• Review of Product accountability and storage.

• Logging and correcting protocol deviations.

• Monitoring study progress.

• Database lock and study close out.