Let Research Assist provide a seamless extension of your staff/company in these areas:
Your clinical trials will be managed in accordance with FDA regulations, ICH guidelines, and GCPs (Good Clinical Practices) to ensure compliance with all regulatory requirements. Your data will be 100% source verified for accuracy, completeness and integrity.
In this competitive field, you need a contract research organization (CRO) that not only ensures the highest levels of quality and integrity, but also provides efficient solutions to your product development needs.
Research Assist can help you meet your specific goals effectively and efficiently. With over 20 years of experience across most therapeutic areas, we provide a full range of clinical trial management services to the industry (pharmaceutical, biotechnology, medical device and diagnostic).
In order to meet your specific research needs, we offer different levels of support, including in-house contractors, expert consultants or complete management of your clinical project(s).