Services Overview

Outstanding quality, professionalism and expertise – the high standards that can be expected from ClinPros. With years of experience in the field, our team is comprised of individuals with the knowledge and expertise that will guarantee that your project is successfully managed.

FULL SERVICE CRO

Quality Assurance

Quality at ClinPros is a way of life – it is ingrained in our culture and reflected in the way we do business. Our commitment to quality means that each clinical study is conducted, recorded, and reported in accordance with clinical study protocol, Standard Operating Procedures (SOP), International Conference on Harmonization (ICH) Good Clinical Practices (GCP), and applicable country or regional regulations.

Project Management

ClinPros partners with you to select the right team leadership from study inception. We recognize every client, study, and team have unique dynamics. Based on your specific needs, we carefully select customized leadership from a highly experienced team of professionals. We identify potential risks specific to your study and manage them proactively with pre-agreed Quality/Risk Management Plans (Incorporated into an overall Project Management Plan).

Our team of Project Managers has an average of more than 20 years clinical trials experience with strong leadership skills.

This experience is evident as they work alongside client teams to develop strategies, maneuver challenges, and drive to meet study goals.

CLINICAL OPERATIONS

Trustworthy, Experienced Partners

The right planning, execution, and ongoing maintenance of your study will ensure its success. ClinPros understands the value of having trustworthy, collaborative, experienced clinical operation team as a critical component to this process. We work through site feasibility activities, perform ongoing monitoring onsite and/or remote, or complete study close-out activities, our knowledgeable clinical operations team members partner with you to reach your trial goals.

Virtual Trials and Remote Monitoring

We conduct virtual trials and remote monitoring to support patient centricity, safety and project efficiency.

FUNCTIONAL SERVICE PROVIDER

With our FSP model, we have capabilities to enable sponsors to outsource specific functional components of a clinical trial to external partner(s) while still maintaining their control over the data and overall process.

CLINICAL DATA MANAGEMENT

ClinPros offers data management and analysis services, including a variety of EDC platforms customizable to meet your needs.

MEDICAL & REGULATORY SUPPORT

Patient rights, welfare and safety are paramount in the process of conducting all our clinical studies.

Our Services

Pharmacovigilance and safety services

Clinical Monitoring and Site Management

Electronic Data Capture (EDC) platforms

Electronic Trial Master File (eTMF) management

Feasibility and start-up support

Investigator meeting planning

Medical monitoring

Patient recruitment support

Functional Service Provider (FSP)

QUALITY ASSURANCE

Quality Is in Everything We Do

Quality at ClinPros is a way of life; it is ingrained in our culture and reflected in the way we do business. Our commitment to quality means that each clinical study is conducted, recorded, and reported in accordance with clinical study protocol, Standard Operating Procedures (SOP), International Conference on Harmonization (ICH) Good Clinical Practices (GCP), and applicable country or regional regulations. Driven by detail, our Quality Assurance (QA) department conducts investigator site audits and provides regulatory authority inspection readiness preparation – additional support to prepare sites for audit readiness is also available. So that nothing is left to chance, QA diligently evaluates vendors to establish that they meet our qualification requirements.

ClinPros study teams collaborate and communicate with sponsor counterparts for full transparency and quality throughout each study. Integrated Quality Risk Management processes and plans are used to develop a risk-proportionate, data-driven approach based on the design of the clinical study. Internally, quality control activities and processes are in place so that ClinPros activities are properly executed. Our independent QA department performs routine assessments of our services to confirm we are compliant with our internal Standard Operating Procedures (SOPs), ICH GCPs, and regulatory authority guidance.

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