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Navigating the Future of Global Clinical Operations
Our Clinical Trial Operations services offer comprehensive support throughout all phases of clinical trials, from Phase II to Phase IV, demonstrating our dedication to orchestrating a seamless project experience from start to finish.
Our Key Differentiators in Global Clinical Operations
Global Reach with Local Expertise
Accelerated Patient Recruitment & Enhanced Retention
Partnership with certified Bioanalytical Lab
Robust SOPs for IP management
Industry-standard e-Clinical Technologies
Global Clinical Operation Solutions
Our multi-faceted approach ensures trial sites are well-equipped, compliant with local regulations, and cater to the target patient population. Our detailed evaluation optimizes trial outcomes and minimizes site selection challenges.
Our Key steps to Site Selection & Feasibility for Maximizing Enrollment Potential:
- Locating facilities with the optimal resources (such as equipment and staff)
- Evaluating the epidemiological landscape and patient demographics
- Tracking historical performance site-by-site
Our skilled clinical research associates (CRAs) are committed to executing all studies with exceptional quality at each site. They work closely with site teams to ensure the delivery of high-quality data, utilizing our established procedures and tools while strictly adhering to global and regional regulations.
Our strategies encompass patient enrolment processes, including effective recruitment and retention techniques, as well as direct-to-patient referral strategies. We prioritize patient awareness and support to facilitate ease of participation and compliance.
Patient Recruitment Methods:
- Advocacy groups
- Referrals from Healthcare Providers (with Doctor/KOL involvement)
- Volunteer Education
- Study information sheets
- Facilitating Informed Consent
- Patient Registries
Patient Retention Methods:
- Preparing scripts to address common questions from prospective participants
- Continuous guidance and assistance from in-house Clinical Trial Specialist
We begin the process by developing a detailed monitoring plan that specifies all relevant information. By adopting a data-driven approach, we can customize our monitoring strategies to meet the specific needs of each study and make adjustments based on-site performance and activity.
Diverse Functions of Our Clinical Trial Monitors:
- Routine Monitoring
- Safety Monitoring
- Compliance Documentation Monitoring
- Risk-Based Monitoring
- Regulatory Compliance Monitoring
From Start-Up to Close-Out: Key Technologies Driving Clinical Operations
Request for Proposal
Let us take your clinical trials global? Contact us today to learn how we can support your clinical development journey with our comprehensive global trial operations.