Clinical Research Expertise
Abdominal Bulging
Acne
Actinic Keratosis
Allergic Subjects
Alopecia
Atopic Dermatitis
Cheek Augmentation
Chronic Low Back Pain
Common Warts
Diabetic Foot Infections
Fibromyalgia
Gastric Ulcers with OA
Gout
Hand Eczema
Hyperhidrosis
Influenza Vaccine
Lips & Cheek Augmentation Fillers
Lupus
Melasma
Meningococcal Vaccine
Nasolabial Folds Filler
Notalgia Paresthetica
NSAID
Onychomycosis
Osteoarthritis
Palmoplantar Pustulosis
Patch Testing
Pneumococcal Vaccine
Pruritus
Psoriasis
Psoriatic Arthritis
Rheumatoid Arthritis
Rosacea
Sarcopenia
Seborrheic Dermatitis
Seborrheic Keratosis
Solar Lentigines
Traveler’s Diarrhea
Tinea Corporis
Tinea Cruris
Tinea Pedis
Vaginitis & Vaginosis
Venous Ulcers
Vitiligo
West Nile Virus
Zostavax Vaccine
Our centers include:
Lobby and reception area
Examination rooms
Phase 1 unit with beds, shower and breakroom for inpatient overnight studies.
Temperature monitored pharmacy room
CLIA certified laboratory
Conference room
Dedicated monitoring space
Administrative and coordinating offices
Archiving space for study records
Designated parking for patients and CRAs
Board Certified Investigators
ACRP Certified Coordinators
Bilingual staff (English & Spanish)
Diagnostic imaging access
Equipped with:
ECG machine
Oxymeter
Sphygmomanometer
Ambient & refrigerated centrifuges
Dry incubator
Microscope
-20°C & -80°C freezers
2°C to 8°C locking refrigerator
Emergency medication
Oxygen
Defibrillator
24/7 temperature-monitored IP room
Security and fire alarm system
Back-up power generators
High speed Internet, telephone, and fax service
Personnel trained on:
Good Clinical Practice (GCP)
Protection of Human Research Subjects
Handling for Transportation of Dangerous Goods (IATA)
Cardiopulmonary Resurrection (CPR)
Standard Operating Procedures (SOPs)
Health Insurance Portability and Accountability Act (HIPAA)
Occupational Safety and Health Administration (OSHA)
Electronic Data Capture System (EDC)
Interactive Web Response Systems (IWRS)
Medical Photography
Electronic patient-reported outcomes (ePRO)
Driven Research International LLC serves as a liaison between our partner sites in the US/Latin America and Sponsors/CROs for phase 1, 2 & 3 clinical trials , including the capability for inpatient studies.
Services provided include:
Site Qualification & Personnel Training
SOP Development, Revision & Implementation
Site Feasibility Support
Study Start-Up
Regulatory Support
Contract & Budget Negotiations
Site Payments
Monitoring Support
Source Documents Development
Logistics Support
Quality Assurance
Certified Translations
Archiving