All services are offered either at research grade or in compliance with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (GMP) promulgated by the US FDA, OECD, European Commission (EC), Japanese, and other international regulatory agencies.
CGMP (Current Good Manufacturing Practices) are the practices required in order to conform to the guidelines recommended by agencies that control the authorization and licensing of the manufacture and sale of pharmaceutical products, and medical devices.
GLP (Good Laboratory Practice) ensures scientific data integrity is being protected at the research level and is applicable for experimental or non-clinical studies conducted for the assessment of the safety or efficacy.
Any of our services are also available at research level with a reduced cost. Research level testing is completed without quality assurance oversight and is not appropriate for submission to regulatory agencies.
When you partner with Avance Biosciences™, you gain a CRO partner that is creative, collaborative and dedicated to sound science with a focus on the regulatory requirements our partners require. Contact our technical staff to discuss how we can support you in your project!
