At MedNet Solutions, we are dedicated to providing the highest quality training and supportive services possible to help our customers succeed and to ensure they get the most out of thier technology.
Successfully manage your clinical development programs.
Our security and governance capabilities, including ISO 207001 certification, FDA 21 CFR Part 11 validation and HIPAA compliance, were designed to protect high-value information for the most-regulated industries.
Streamline real-time data access and analysis with iMedNet's Report Manager.
Clinical operations are a critical component in all studies. SynteractHCR’s highly skilled staff is well-versed in clinical trial operations including implementing, monitoring and managing the clinical components of a study. From start-up to close-out, experienced clinical managers and clinical research associates (CRAs) oversee each study’s clinical processes to ensure proper planning, conduct, patient safety, and data quality, while fostering good communication between study sites and sponsor.
TrialMax Web™ is a web-based diary specifically designed for late phase trials, which tend to be larger and longer in duration.
We will collaborate with you to design a customized base IRT system that meets your unique requirements.
Our dedicated logistics facilities in Europe and North America, coupled with our expertise in negotiating the challenging import processes, enable us to provide timely and reliable delivery throughout the study into any part of the world. This ensures even the most actively recruiting sites always have the diary devices they need.
TrialMax Touch™ is a handheld diary that can be used by patients at home or by the caregiver. TrialMax is a software platform that provides a single solution for eCOA (electronic Clinical Outcome Assessments) in Phase I to IV clinical trials.
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