They meticulously review the following documents:

·     The informed consent document content.

·     The documents concerning interactions with the IRB. 

·     The documents and procedures concerning drug accountability. 

·     Accacia Serum’s staffs inspect facilities and equipment. 

·     The quality assurance personnel review that the data collected in a representative sample of Case Report Forms are authentic and supported by source documents. 

·     Records and procedures for site visits are reviewed. 

·     Assess compliance with internal Standard Operating Procedures.

Accacia Serum’s staffs’ commitment to quality and services ensures satisfaction from our clients.