KlinEra’s reputation for delivering exacting quality control, accurate data, and a deep understanding of regulatory procedures and protocols, are our most important attributes for our medical monitoring services.
With access to expert professionals with vast experience and KlinEra’s reach in both local and global geographies, we ensure qualified and trained personnel for medical monitoring services are always available to our clients.
Whether you need monitoring throughout an entire clinical trial, or need a critical gap in your team filled, KlinEra’s experienced professionals can fulfill your needs at any level.
Our flexible clinical monitoring services are designed to accommodate all types and phases of a clinical trials, while our personalized communication processes and experienced team of project managers ensure that sponsors receive up-to-date information on all aspects of the trial for the duration of the trial.
KlinEra's project managers have extensive experience in managing global clinical trials and work as a conduit for the sponsor clinical team and the local regional clinical teams.
Our clinical research associates (CRAs) are required to have at least two years of field monitoring experience and be certified in all regulatory guidelines (GCP, CFR, and ICH) and our Quality Control (QC) monitor evaluation process -- which supplements individual monitor training -- ensures the highest quality standards.
KlinEra provides medical monitoring support in the United States, Europe, Southeast Asia, India and Russia.