AmeriTrial's services begin with trial pre-planning with the sponsor's personnel and continues through completion of the trial, site closeout and data submission. The following Phase III & IV services are offered as a complete turnkey trial or as individual, stand-alone trial components.
Phase III-IV Trial Services
- Pre-planning/Study Design
- Protocol Development
- Development Trial Forms/Material
- Regulatory Approval
- Site/Investigator Selection
- Investigator Meetings/Training
- Site Personnel Training
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- Pre Initiation
- Trial Management
- Site Monitoring
- Data Management
- Site Closeout
- Clinical/Statistical Reports
- Quality Assurance Audits
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Therapeutic Areas
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Allergy
Allergic Conjunctivitis
Allergic Rhinitis
Cardiology
Hypertension/Lipid
Hypercholesterolemia
Peripheral Vascular
Cholesterol Lowering
Dermatology
Atopic Dermatitis
Fungal Infections-Antimycotic
Pain Relief
Wound Healing
Gastroenterology
Irritable Bowel Syndrome
Reflux/Heartburn
Ulcerative Colitis |
Infectious Diseases
Skin & Soft Tissue Infection
Urinary Tract Infection
Neuropharmacological
Depression
Metabolism & Endocrine
Dietary Supplements
Hormone Replacement
Rheumatology
Osteoarthritis
Urology
Bladder Control |
Investigator Database
We have a large database of pre-qualified, pre-approved, geographically disbursed Investigator sites. Pre-approval is based on the sites' experience/training; skill of clinical staff; adequacy of site facilities; and ability to enroll patients at the required rate — with emphasis on naive patients.
To be included in AmeriTrial's pre-qualified database, you may submit your Investigator site for pre-approval review by completing a short questionnaire. Just click the link "Investigator Form" and follow directions.
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