CRO Services

Clinical Monitoring At Lotus Clinical Research, our Clinical Research Associates (CRAs) are focused upon the two cornerstone responsibilities of Good Clinical Practice (GCP):  protecting the rights and well-being of human subjects and ensuring that trial data are accurate and complete,..

Our databases fulfill important baseline attributes while allowing for the specialized configuration required for analgesic report outputs, and are configured with the end goal in mind: appropriate calculation of primary and secondary endpoints. Data management services include: In-house database design..

Biostatistics Our biostatistical staff members provide more than data analysis; they have in-depth knowledge of the methods for studying analgesic medications and the techniques that are used to analyze their results. Lotus Clinical Research biostatisticians have years of experience processing..

24-hour safety service. Lotus Clinical Research's team of experienced physicians and nurses is dedicated to providing a support network for our subjects. In order to provide this level of support, Lotus Clinical Research provides a 24-hour safety service for our..

Clinical and Regulatory Writing. Lotus Clinical Research medical writers are experienced in both clinical and regulatory writing techniques to provide concisely written documents. Our writers work closely with our biostatisticians and peer reviewers to ensure documents are complete and faithfully..

Lotus performs compartmental (model-dependent) or noncompartmental (model-independent) pharmacokinetic analysis, using validated Phoenix WinNonlin software. We produce pharmacokinetic reports to support clinical studies.

Comply with protocol and regulatory requirements. Lotus Clinical Research’s quality management team supports our internal teams and clients with the production of documents that comply with protocol and regulatory requirements. Our quality operations management supports the preparation of procedures, reports,..