You are here
Providing independent Quality Assurance services by highly experienced professionals, across all clinical trial phases.
As well as being an integral part of our internal processes, Novotech is able to provide a full range of independent Quality Assurance services from pre-clinical, through phase I to phase IV studies.
Available internationally, a Novotech clinical trial audit ensures high ethical standards of clinical trials are upheld and minimizes risk to data integrity.
Our QA department is staffed by experienced professionals who operate independently from the personnel engaged in the management and conduct of clinical trials.
Quality Assurance services encompass all aspects of the clinical development process, including:
|Trial Master File Audits||Investigator Site Audits|
|Phase I Units||Systems Audits|
|Third party vendors including archive facilities, Investigational Product management and other CROs||Study Documentation e.g. Protocols, Clinical Study Reports|
|Computer System Validation Reviews||Local, Central and Bioanalytical Laboratories|
|Database Audits||GLP Audits|
|Bioanalytical Method Validation||Quality System Management|
Our auditors have extensive auditing experience in various types of clinical trial audits. Audits have been performed for a wide range of indications and in various countries e.g. US, Canada, South America, Western, Central and Eastern Europe, India, Thailand, Australia and New Zealand.