We recognize that Project Management is the bedrock of a successful clinical study.
Our monitors (CRAs) attend in-house education courses and are kept up-to-date with the latest information on current and upcoming developments.
We assure compliance with ICH GCP and relevant national/international regulations.
One of the primary reasons our Data Management system activities are run on globally proven and specialized software like Oracle.
QUINTESSENTIAL’s biostatisticians have extensive knowledge of statistical methodology for drug and device development.
To provide medical writing of the highest quality, our projects are headed by an experienced research person.
QUINTESSENTIAL provides the comprehensive services of unique site management and clinical monitoring capabilities.
QUINTESSENTIAL provides service for Phase IV clinical trials which conducted for identify and evaluate.
QUINTESSENTIAL’s Commercialization & Outcomes practices provide insights to clients on strategies and execution.
Pharmacovigilance encompasses surveillance of adverse events after short-term and long-term use of medicines.
QUINTESSENTIAL offers a broad range of early development services, including drug discovery and development.
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