We are thrilled to announce an upcoming joint webinar, “Speeding Up Patient Recruitment with Automated Site Payments,” presented by Flex Databases and Confidence Pharmaceutical Research.
On June 1st at 12:00 EST/18:00 CET, this live discussion will delve into the significance of site payments in study management and highlight the streamlined site payment process at Confidence Pharmaceutical Research. Join us for an insightful session featuring real-life case studies, including a remarkable example of how a leading pharma company accelerated site payments by 8 times using our automated site payment services.
Date: June 1st
Time: 12:00 EST/18:00 CET
Duration: Approximately 1 hour
Key Topics to Be Covered:
- Understanding the Importance of Site Payments in Clinical Trials
- Explore how timely and accurate site payments positively impact study management and participant recruitment.
- Discover the Efficient Site Payment Process at Confidence Pharmaceutical Research
- Gain insights into Confidence Pharmaceutical Research’s approach to automating site payments, optimizing efficiency, and ensuring compliance.
- Real-Life Case Studies: Transforming Site Payment Speed and Accuracy
- Uncover success stories, including a big pharma company’s experience of accelerating site payments eightfold through our automated site payment services.
Attendees will have the opportunity to engage in a live Q&A session following the presentations. This interactive segment allows you to address any inquiries or concerns you may have about automating site payments in clinical trials.
Register now to reserve your place among industry experts, professionals, and stakeholders who are passionate about optimizing the clinical trial process.
We look forward to seeing you on June 1st.
About Confidence Pharmaceutical Research
Confidence Pharmaceutical Research, founded by clinical research pioneers Dr. Serge Varshavsky and Dr. Efim Kelman, is a private full-service Contract Research Organization with a multifaceted, innovative approach to clinical trials. Our experienced professionals have conducted trials sponsored by small and mid-sized biotech and large pharmaceutical companies, medical device companies, as well as with governmental grants and academic research organizations, completing studies in over 35 countries across the world.
We maintain a high level of consistency and quality through our comprehensive set of standard operating procedures, forms, templates, and documentation. Our executives, who are medical doctors and respected trialists, have built a peer-to-peer network with leading clinical investigators in all areas of medicine and clinical research to ensure fast and reliable patient enrollment. With proprietary tools, systems, and processes, our feasibility team can identify ideal study sites and propose an optimal mix of study sites for any therapeutic area, including rare diseases and large-scale global outcome studies.