Revolutionizing Medical Research
Site Feasibility & Trial Readiness Assessment
Site Feasibility & Trial Readiness Assessment
Site Feasibility & Trial Readiness Assessment
Assess your site's capacity and readiness to conduct specific trials, ensuring the necessary infrastructure, staffing, and resources are in place.
Regulatory Compliance & Quality Assurance
Site Feasibility & Trial Readiness Assessment
Site Feasibility & Trial Readiness Assessment
Provide guidance on regulatory requirements (FDA, EMA, ICH-GCP), prepare for audits, and conduct regular compliance checks to minimize risks and ensure high standards.
Budget & Negotiation Support
Site Feasibility & Trial Readiness Assessment
Clinical Trial Management Support
Assist with budget development, cost management, and contract negotiations with sponsors and CROs to ensure fair terms and financial optimization for your site.
Clinical Trial Management Support
Patient Recruitment & Retention Strategies
Clinical Trial Management Support
Offer project management guidance, staff training, and risk management strategies to ensure trials run smoothly and meet timelines and budgets.
Patient Recruitment & Retention Strategies
Patient Recruitment & Retention Strategies
Patient Recruitment & Retention Strategies
Develop tailored recruitment strategies, retention plans, and inclusive practices to enhance patient engagement and reduce dropout rates.
Source Document Creation & Management
Patient Recruitment & Retention Strategies
Patient Recruitment & Retention Strategies
Support the creation and management of compliant, organized source documents, ensuring data integrity and readiness for audits and regulatory inspections.
Investigator & Staff Training
Investigator & Staff Training
Investigator & Staff Training
Provide customized training programs for site staff on GCP, protocols, patient safety, and regulatory requirements, ensuring ongoing professional development.