Clinical Research Site Support Services
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What We Offer
After reviewing your site's performance WilMar Clinical Consulting can tailor a plan to increase compliance and proficiency at your site. We do this by providing the following services, as well as additional services if needed.
✔️ Performance Guidance
Working with CRCs to hone skills and improve performance while adhering to ICH-GCP guidelines; assisting with creating tools to maintain up-to-date regulatory document compliance
✔️ Staff Training
Training provided for staff personnel regarding their role at the site. Protocol specific training is provided as well.
✔️ Source Document Assistance
Assisting with the creation of source documents and providing guidance on source document creation
✔️ Monitoring Visit Preparation
In preparation for Interim Monitoring Visits conducted at your site we provide:
- Quality Assurance (QA) services
- Detailed review of source documents and CRFs/eCRFs for compliance
- Review of queries (answered and unanswered)
- Review of IP records
- Review of Investigator Site File (ISF) to confirm regulatory compliance
✔️ Scalable Solutions
WilMar offers customizable services based on your needs and budget.