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  • Current Trials

SPONSOR/ CRO INFORMATION

Thank you for your interest in our Site Management Organization (SMO), Clinical Research Professionals.  We are dedicated to the ethical and professional management of Clinical Trials.  All members of our clinical team are medically trained and certified.  All coordinators are CCRC certified.  Quality and integrity of data is our leading value. Our clinical trial sites are in the Investigator’s office which promotes optimal Investigator oversight of the trial.  Additionally, medical records are more readily available for clinical trial subjects.  All of the professional team has been trained extensively in FDA and ICH Guidelines.  We have dedicated specialists to accurately complete budgets and contracts and regulatory submissions in a timely manner.  A regulatory submission can be completed in as little as 3 days. An average time for a contract and budget is 7-10 days.  A dedicated recruitment specialist team assures successful enrollment of each trial.  Be assured that we are committed to excellence.
Please click this button to fill out the registration and one of our clinical research professionals team members will contact you. We look forward to working with you for all of  your research needs.
Sponsor/ CRO Signup

SERVICES
Please visit our services page for more information



Clinical Trial Management
Employee Training

Employee Mentoring
Safety Monitoring
Archiving Services
Data Analysis



Monitoring
SOP Creation
Audit Support
Regulatory Filing
Budgeting
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EXPERIENCE
Our experience includes phases 2-4 in the following therapeutic areas
Migraine Headaches
Insomnia
Alzheimer’s Disease
Memory Impairment
Restless Leg Syndrome
General Anxiety Disorder
Depression
Hyperlipidemia
Hypertension
Coronary Artery Disease
Diabetes – Type I & II
Obesity
Osteoarthritis
Oncology
Pain
Male Sexual Dysfunction
Female Sexual Dysfunction
Overactive Bladder
Heartburn
IBS
Nocturia
Vaccines
Parkinson's Disease

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We look forward to an opportunity to work with you and your team to help you achieve your objectives and exceed your goals.
To View Our Clinical Trial Experience Click Here
Trial Experience
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©Clinical Research Professionals (CRP) 2014
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