Clinical and Regulatory documents are essential for drug development and management of approved drugs. QARA PHARMA was founded to fill an existing void, providing a superior document management system to help the pharmaceutical industry prepare and submit optimal documents. We have assembled a team of experienced medical writers and physicians to facilitate your goal of creating clinical and regulatory reports that meet the highest standards in the industry.
To build a center of excellence to create and maintain exceptional clinical and regulatory documents associated with Product Development and Medical Affairs
Dedicated to meeting the needs of the bio-pharmaceutical industry through open communication to reduce time to market, manage risk and fulfill all regulatory requirements.
We provide comprehensive services, customized to assist bio-pharmaceutical companies with the successful preparation and completion of clinical documents and regulatory dossiers to fulfill global regulatory agency requirements.
We are unique, offering comprehensive services beyond writing, including substantive review and editing by experienced clinicians. Our expertise will immediately fill any gap in your development cycle.