Our Services
Full-service clinical research delivery.
From site feasibility and study start-up through to close-out, Zentric provides the expertise, infrastructure and commitment to deliver your clinical program to the highest standards.
Phase 1–4 Clinical Trials
Early-phase through late-phase study delivery.
Zentric is equipped to support the delivery of early-phase through late-phase clinical studies across a broad range of therapeutic areas. Our experienced site team understands the demands of each phase and is committed to quality delivery.
- Phase 1 first-in-human and dose-escalation studies
- Phase 2 proof-of-concept and dose-finding studies
- Phase 3 pivotal and confirmatory trials
- Phase 4 post-marketing and observational studies
Site Feasibility & Start-Up
Efficient assessment and trial readiness.
We provide thorough and responsive site feasibility assessments, ensuring your study can be initiated efficiently. Our start-up processes are designed to minimise delays and get your trial underway as quickly as possible.
- Rapid feasibility assessment and response
- Site initiation and staff training
- Regulatory and ethics submission support
- Site readiness and infrastructure review
Participant Recruitment & Retention
A participant-focused approach to enrolment.
Successful clinical trials depend on recruiting and retaining the right participants. Our team takes a thoughtful, participant-centred approach to recruitment — prioritising genuine engagement, clear communication and ongoing support.
- Targeted participant identification and screening
- Community and referral network engagement
- Participant communication and support throughout
- Retention strategies tailored to study requirements
Clinical Trial Delivery
Professional site management across the study lifecycle.
Our site team manages all aspects of clinical trial delivery — from protocol implementation through to study close-out. We are committed to quality, compliance and clear communication with sponsors and CROs throughout.
- Protocol implementation and compliance
- Investigational product management
- Source data and regulatory documentation
- Monitoring visit support and query resolution
Sponsor & CRO Collaboration
Responsive partnership throughout your program.
We understand that sponsors and CROs need a site partner they can rely on. Zentric is committed to responsive communication, proactive problem-solving and close collaboration to support the success of your clinical program.
- Dedicated point of contact for sponsors and CROs
- Proactive communication and issue escalation
- Flexible and responsive to sponsor requirements
- Regular progress reporting and updates
Quality & Compliance
A strong foundation of quality and regulatory compliance.
Quality is embedded in everything we do at Zentric. Our processes are designed to ensure protocol compliance, participant safety and full adherence to regulatory and GCP requirements throughout every study.
- GCP-compliant processes and documentation
- Protocol deviation prevention and management
- Participant safety monitoring and reporting
- Audit readiness and inspection preparation
Therapeutic areas.
Ready to discuss your study?
Contact our team to discuss your clinical program and how Zentric can support your research.
Contact Our Team