Comprehensive Clinical Monitoring Services

Find and resolve issues early with complete clinical trial monitoring, co‑monitoring, and site management services that ensure drug accountability, data integrity, and trial efficiency.

  • Qualification, initiation, routine, and close‑out visits and reports
  • Thorough review of site records and monitor reports
  • In‑country expertise for feasibility and regulatory submissions
  • Site management support, documentation, and training
  • Source document verification and periodic remote database review

Risk‑Based Monitoring That Works

Optimize resources and maintain quality through our industry‑leading risk‑based clinical trial monitoring services.

  • Multi‑site comparisons and data centralization to identify outliers
  • Early risk detection and immediate solution development
  • Higher‑quality data at a lower cost
  • Streamlined approach increasingly preferred by regulators
  • Scalable solutions to support trials of all sizes

Local Experts, Global Excellence

Gain access to specialist knowledge and established relationships for exceptional patient recruitment and retention and smooth trial execution, wherever your study is taking place.

  • Experienced teams of regional clinical research associates (CRAs)
  • Diverse expertise, including in renal, cardiometabolic, and oncology
  • Committed to data quality, patient safety, and issue resolution
  • Hybrid approaches combining remote and on‑site monitoring
  • Strong relationships with key opinion leaders and investigators

Site Management for Seamless Trials

We simplify site operations through expert management, training, and documentation, ensuring your trials run efficiently from start to finish.

From site selection and feasibility assessment to trial closeout, you can be confident in our Good Clinical Practice (GCP)-compliant clinical trial monitoring services.

Our comprehensive clinical site management services integrate quality assurance mechanisms throughout. We develop recruitment criteria, manage patient recruitment, and ensure timely, thorough communication with sites. We also provide training tailored to your study’s needs and oversee local ethics review processes.

Case Study

Robust Clinical Monitoring Services

When tasked with supporting a Phase III rotavirus vaccine trial, we navigated complex logistics and an outpatient pediatric population to deliver seamless clinical trial monitoring services.

  • Efficient site initiation across all locations within two weeks
  • Strong site relationships to support rapid recruitment of 2,000+ participants, surpassing targets
  • Precise monitoring of strict cold chain requirements
  • No critical findings from site audits and regulatory inspections

We helped pave the way for vaccine licensure—bringing the world closer to protecting millions of children from life‑threatening rotavirus.

See our impact in action

Frequently asked questions

What is risk‑based monitoring, and how can it benefit my trial?

Risk‑based monitoring is a more efficient way to oversee your clinical trial. Focusing on the critical data and processes that matter most for patient safety and data quality helps us identify potential issues early, resolve them quickly, and keep your trial running smoothly.

With centralized dashboards, we can compare data across sites to spot errors, outliers, or unusual patterns, reducing the risk of missed issues. This allows us to target on‑site audits where needed most, saving time and money while ensuring accuracy and confidence in your trial results.

What steps do you take to ensure compliance with evolving regulations?

We monitor regulatory changes globally and adapt strategies to maintain compliance so that we can continue to deliver industry‑leading clinical trial monitoring services.

Our dedicated team stays updated on evolving standards, liaises with local authorities, and proactively adjusts documentation, processes, and timelines so you can be confident that your trial aligns with the latest requirements in every region.

What technology do you use for data capture and monitoring?

Our highly trained teams use fully validated, 21 CFR Part 11 compliant electronic data capture (EDC) systems, including Medidata Rave®, Zelta™, and other industry‑leading systems, enabling efficient data management and real‑time monitoring for your data integrity and security.

How do you ensure effective clinical trial monitoring services across different regions?

We combine local expertise with global reach to deliver clinical trial excellence. With teams on the ground in 40+ locations in APAC, Europe, and the USA, we bring a deep understanding of local languages, cultures, and regulations to every study.

This localized knowledge ensures seamless site monitoring, faster trial start‑ups, and culturally sensitive patient engagement while maintaining the highest global standards of quality and compliance.

Related Services

Study Design & Start‑Up

Partner with us to create custom, cost‑effective trial strategies that meet regulatory and sponsor requirements, regardless of project complexity.

Patient Recruitment

Accelerate recruitment and boost retention through our established global alliances with trusted sites and investigators, including a strong APAC presence.

Project Management

Drive clinical research success with our experienced project management team, seamlessly coordinating functional areas and vendors across the trial lifecycle.

Endpoint Adjudication

Generate reliable, unbiased data and advance your study with support from global experts and efficient workflows tailored to every program.