Why Partner with KPAR?
Experience Matters
- Participation in over 500 Phase I-IV clinical trials.
- Enrolled more than 17,000 participants.
- Have worked with most major pharmaceutical sponsors.
- Contributed to licensure of almost all pediatric and adult vaccines, antibiotics, ADHD treatments, and many more.
- Consistently meets enrollment expectations, often exceeding.
- Accurately and transparently estimates enrollment ability, enabling sponsors to plan and depend on enrollment at our site
- Can accommodate rapid study start up, 2 week turn around time from receipt of regulatory documents, contract/ budgets to to submission.
- Can partner with any central IRB.
Our Team
- Our Principal Investigator is involved in all aspects of the clinical trial process on a daily basis, easily demonstrating oversight.
- All members of our team maintain GCP certification
- All research nurses and study coordinators are IATA certified
- Extensive experience in phlebotomy, including pediatric phlebotomy. Our research nurses obtain and process all lab samples, integrating the entire patient visit into a cohesive, efficient experience for our volunteers.
- All providers of Physicians to Children & Adolescents are included as Investigators on all trials, allowing integration of the pediatric practice with
Our Reputation
- Retention rates consistently 95% and above.
- Screen Failure rate less than 5%,
- Carefully choose our participants based on their ability to complete all visits and follow study requirements,
- Proven 30+ year track record for meeting and exceeding enrollment expectations.
- Investigators and COO often consulted for protocol development and best operating practices.
Investigator Involvement
- KPAR is well integrated into the daily operations of PTCA. All PTCA providers are Investigators on all trials we conduct.
- Investigators are involved early in the recruitment and enrollment process.
- Our Principal Investigator is available daily to provide oversight, training and meet with monitors.