Corealis’ world-class facilities are custom built to develop and manufacture oral solid dosage (OSD) products
Corealis strictly adheres to current good manufacturing practices (cGMP) in all operations and are compliant with International Council on Harmonisation (ICH) guidelines.
The Corealis Quality Assurance team is made up of experienced scientists with a wealth of knowledge in cGMP analytics and manufacturing operations. The company’s quality systems undergo regular review by auditors and qualified quality persons (European QP).
A recent review conducted through a comprehensive audit by a QQP auditor, eliminates the need for repeated audits during European clinical supply manufacturing campaigns.
This streamlined process saves time, ultimately delivering greater cost value to clients.
