CLINICAL TRIAL SITE SERVICES
MEDICAL SCIENCE LIAISON SERVICES
Our Clinical Trial Site Services Include:
• Site Evaluation
• Site Set Up or Site Process Improvement
• Clinical Research Training
• Contract Negotiations
• Site Budget
• Regulatory
• Pharmacy Training/Set Up
eConsent Service (eCaaS)
Empower researchers with tools for distant screening and participant recruitment, ensuring regulatory adherence.
eCOA & ePRO
Permit healthcare professionals to digitally gather data from patients, including surveys, diaries, and questionnaires.
Trial Assistant
Streamline remote participant screening for clinical trials, resulting in decreased expenses and faster enrollment.
TeleVisits & VideoVisits
Reduce logistical hurdles for researchers and lessen the need for patients to physically visit research sites by providing audio and video call options.
Multiple Channel Patient Interaction
Engage with patients flexibly through diverse mediums like SMS, email, voice, video, and a dedicated study application.
Adverse Reactions & Concurrent Medications
Document any adverse reactions using the MedDRA system and concurrent medication data via WHODrugDB.
Scheduling Visits
Efficiently set up trial visit timetables at centralized venues and make straightforward changes to the protocol.
