Experience
Our project team has developed a wide range of knowledge in their 25 plus years of working in the pharmaceutical/biotech/medical device industry. With an understanding of all phases of human clinical trials (Phases I, II, III, IV) and NDA submissions to the FDA, we are uniquely positioned to partner with clients at any point of their product development. With this experience and expertise, we are able to apply a variety of creative solutions and techniques to whatever a client situation demands. ClinDART strives to be a partner which brings value, good judgment and expertise to the clinical trial process.
Technical Expertise
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Analytics
SAS -
Safety
Argus Safety (Oracle)
ARISg™ (Aris Global) -
Clinical Data Management
Medidata Rave ® Oracle ® InForm Oracle ® RDC Onsite iMedNet ™ Medrio BioClinica
(Electronic Data Collection) -
Clinical Data Management
Oracle ® Clinical (Oracle)
(Paper Studies)
Therapeutic Areas of Knowledge
- Alzheimer’s
- Cardiovascular
- Diabetes/DPN
- Gastrointestinal
- Gynecologic (Endometriosis)
- Immunology
- Infectious Diseases (HIV/AIDS, Dengue Fever, HFMD, Rhino Virus, Malaria)
- Insomnia
- Neurologic Disorders (Multiple Sclerosis, Tardive Dyskinesia, Tourette Syndrome)
- Obesity
- Ocular
- Oncology (Solid Tumor, Hematologic)
- Orthopedic Devices
- Pain/Inflammation (Rheumatoid Arthritis, Endometrial Pain, Acute Pain, Chronic Pain)
- Psoriasis
- Psychopharmacology
- Pulmonary (Asthma, COPD)
- Sexual Dysfunction
- Sickle Cell Anemia
- Virology