With 56% of the world’s population residing in Asia, it is an attractive destination for clinical trials. However, maintaining the quality and integrity...
An auditor should provide a clear and concise report relating to an audit to demonstrate and explain all non-compliances observed during the audit. ...
Although medicinal products for use in adults undergo extensive pharmacological, stability and toxicological testing through clinical trials, this same approach has not always...
Two new GVP modules were published in December 2012, Module III - Pharmacovigilance Inspections and Module IV - Pharmacovigilance Audits, bringing the total...
