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.
SERVICES
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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 |
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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 |
We look forward to an opportunity to work with you and your team to help you achieve your objectives and exceed your goals.
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