The clinical pharmacology team at Lice Source Services has extensive experience in the design, implementation and interpretation of clinical pharmacology studies in the head lice therapeutic area. We have the technical expertise and strong recruiting to complete your clinical trial. Our clinical operations team is experienced in the unique needs of trials (Phase 1-4) for treatment, prevention, diagnostic and screening of head lice. Convenient access to our multi-site Lice Cleanique Research Facilities allows us to provide expert, regulatory-ready data analyses and multiple demographic reports to our clients.
From start to finish, our process is conducted professionally
and efficiently in our state-of-the-art research sites.
Lice Source Services Provides:
Quick start with fast enrollment
Trial planning and design
Comprehensive case report forms
Experience with design of electronic Case Report Forms (eCRFs)
Experience using Electronic Data Capture (EDC) systems.
Informed consent forms available in multiple languages
IRB reviews conducted locally in a timely manner
Standard Operations consistent with regulatory requirements
Lice comb studies
GCP certified staff
Graphical display and tabulation
Interpretation and analysis of study data
Preparation and testing of in vitro formulations
Full HD Video (for trials)
Our fully-equipped laboratory includes:
Freezer to store blood for pharmacokinetics
Micro-video & picture stills (for In vitro studies)
Click play to view video footage filmed in our on-site research lab.