Medical Monitoring Services for Clinical Study Preparations
Safety and compliance are essential for clinical trials, which require the oversight of an experienced medical monitoring team.
Many companies, regardless of industry experience, need medical monitoring support when preparing for clinical trials. At ProPharma Group, our team evaluates your medical monitoring system to ensure there are no pharmacovigilance medical monitoring bandwidth issues, and partners with you to ensure you have the right resources to keep your clinical trials on schedule. Contact us to learn about our medical monitoring services, or read on for additional information.
Our Medical Monitoring Services for Clinical Trials
ProPharma Group’s medical monitoring consultants help you meet requirements to maintain quality and compliance throughout your clinical trials. Our medical monitors have vast knowledge in a wide variety of therapeutic areas and partner with you to address all your needs, including:
- Inclusion/exclusion criteria issues
- Protocol exemptions and deviations
- Medical crisis monitoring for cases involving a study patient
- Medication issues
- Laboratory findings
- SAE reporting
- Causality assessment discussions
Our medical monitoring consultants will work with you to ensure safety and compliance throughout your clinical trials, from pre-trial planning through end-of-trial review. Contact us to learn more about our medical monitoring services and how we can provide expert guidance for your upcoming clinical trials.