About Us
Who we are...
The clinical research industry is one of the most heavily regulated fields, with strict adherence required to guidelines and regulations set forth by regulatory authorities, such as the FDA, EMA, MHRA, and ICH. Non-compliance can lead to severe consequences, including halted trials, legal ramifications, and delays in bringing new drugs and medical devices to market for the patients that are in need.
With over 20 years of experience in clinical and preclinical research, CRC is positioned to partner with life science organizations to implement and maintain robust quality systems and operational oversight. Our tailored approach supports all phases of pharmaceutical development and clinical trials- from toxicity studies through product approval and post-marketing surveillance. Our sole purpose is to support the advancement of safe and ethical clinical research by evaluating studies for adherence to the highest standards or regulatory compliance.