KlinEra stands for ‘Clinical Era’, and the ‘Sinus Rhythm’ above our name expresses our passion for monitoring the pulse of the latest developments in clinical research practices and bringing innovative and cutting-edge therapeutic solutions to the world.
KlinEra was established in 2005 to provide innovative & customised clinical trials/research services. We endeavour to conduct ethical & efficient clinical trials that will accelerate the delivery of novel therapeutic treatments to patients with a quicker time to market for our clients. We feel pride in mentioning that we have a 100% Regulatory approval track record over the last 5 years.
The structure of KlinEra is divided into distinct divisions like project management, clinical operations, regulatory affairs, Pharmacovigilance, clinical trial supplies, quality assurance, and Data management & biostatistics.
The project management team deals with project planning, project kick-off, training, reporting & oversight, vendor mobilization and management. The clinical operations team are responsible for developing & executing the study protocol, recruiting & enrolling patients, collecting & managing data, and providing statistical analysis. Regulatory affairs team are responsible for ensuring that the study complies with all applicable regulations, such as those related to Good Clinical Practice (GCP) and the International Conference on Harmonization (ICH).
KlinEra is well-known in the industry for providing reliable, accurate, error-free data through its robust quality management. As a full-service clinical development provider, we strive to cater to patients’ needs to improve their health & quality of life and to deliver a world-class service.
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