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Clinical Services: Servic Name
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Experienced Clinical Research Associates (CRAs)
Highly trained with deep scientific and clinical expertise, our CRAs thoroughly understand your investigational product, protocol, and regulatory landscape.
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Rigorous Clinical Trial Oversight
Our meticulous monitoring ensures trial data accuracy, completeness, and traceability, while maintaining strict adherence to protocols, GCP, and regulations
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Proactive Communication with Sites
Our team maintains constant communication with site staff to ensure timely data entry, resolve queries, and address any issues that arise during the trial.
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Customized Monitoring Plans
Our tailored monitoring plans outline specific monitoring methods, responsibilities, and requirements, addressing the unique risks and needs of your study.
Proxima's COmprehensive Monitoring approach
Our comprehensive monitoring approach includes on-site and remote visits, data verification, and detailed reporting.
We focus on identifying and mitigating risks, ensuring subject safety, and maintaining data integrity throughout the trial. Our monitors are adept at recognizing potential issues early and providing actionable insights to keep your trial on track.
We focus on identifying and mitigating risks, ensuring subject safety, and maintaining data integrity throughout the trial. Our monitors are adept at recognizing potential issues early and providing actionable insights to keep your trial on track.
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EARLY CLINICAL DEVELOPMENT
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CLINICAL CRO DELIVERY
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CONSULTING
Process Option 2
Our team of therapeutic and operational experts can support all aspects of clinical and commercial operations, allowing for easier innovation and earlier access to market.
Our trial delivery focuses on agility, efficiency, speed, and a deep understanding of cardiovascular endpoints. We work with class II and class III devices, whether they support a 510(k), PMA, post approval, or observational assessment.
Our trial delivery focuses on agility, efficiency, speed, and a deep understanding of cardiovascular endpoints. We work with class II and class III devices, whether they support a 510(k), PMA, post approval, or observational assessment.
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