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Project Management and Monitoring

  • Comprehensive Project Planning: We work closely with our clients to create a comprehensive service plan tailored to their needs. Our Project Managers define key tasks, timelines and deliverables, ensuring effective coordination and communication between all stakeholders.

  • Study Protocol Review: We conduct extensive research on curriculum to ensure that they are scientifically sound and comply with regulatory requirements. Our team identifies potential risks, challenges and optimization opportunities, providing valuable insights for study design and implementation.

  • Site Selection and Feasibility: We assist in the selection of research sites by conducting in-depth research. Our team considers factors such as patient population, infrastructure, regulatory compliance, and logistics capabilities to determine the most suitable study site.

  • Clinical Site Management: We provide full supervision and control of the clinical research site throughout the study. Our on-site team members receive the training, resources and support necessary for a successful study. We encourage effective communication between sponsors, researchers and research teams.

  • Data Collection and Quality Control: We implement a rigorous data collection process and ensure the highest standards of data quality are available. Our team develops comprehensive data collection tools, monitors data collection processes, and conducts regular data audits to ensure accuracy and completeness.

  • Risk Management: We conduct risk assessments and develop risk mitigation plans to minimize potential problems that may affect studies. Our team actively identifies and communicates various risks related to patient recruitment, data integrity, regulatory compliance and study practices, ensuring the smooth progress of the project.

  • Site Monitoring: We regularly conduct on-site monitoring visits to ensure compliance with study protocols, regulatory requirements and Good Clinical Practice (GCP). Our reviewers check data accuracy, monitor site performance, and provide ongoing training and support to researchers and research teams.

  • Progress Reporting: We regularly provide clients with progress reports, keeping them informed of study milestones, enrollment rates, data quality, and anything else that matters. Our team ensures clear and timely communication throughout the project.
Contact Us

At Althian we understand the critical role of site feasibility and patient recruitment planning in the success of clinical trials. Our dedicated team of professionals utilizes industry best practices and innovative strategies to identify suitable sites and implement effective patient recruitment plans.

Partner with Althian for reliable, efficient, and compliant clinical research services in Mexico. Contact us today to discuss your specific needs and start your journey towards successful clinical trials.

Expertise and excellence, delivering reliable, superior results

Look no further than Althian, a leading company specializing in a wide range of clinical research services.

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