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ClinAudits Joins Bioanalytical Quality Standards Initiative (BQSI) Expert Working Group
Date:3/18/2010

he productivity of their clients. For example, ClinAudits provides Clinical Trial Supply audits, but does not conduct or manage clinical trials, further justifying its objectivity and independence. ClinAudits performs multiple types of audits in GCP, both domestically and internationally including but not limited to investigator sites, CRO (pre-qualification or post capability), IRB, final study reports, central labs, phase 1 units, computer validation, mock FDA/EMEA, pharmacovigilance and database audits. For more information about the pharmaceutical auditing services and quality remediation solutions provided by ClinAudits, visit www.clinaudits.com/about.htm.

About BQSI
Companies interested in becoming BQSI Expert Working Group members can contact Dr. Kirk Smith by email at ksmith(at)synomicspharma(dot)com, or by calling Synomics Pharma at 508-273-0450. Interested parties may also join the BioAnalytical Quality Standard Initiative (BQSI) Group on LinkedIn. A white paper, titled “BioAnalytical Quality Standard Initiative — Implementing ICH Q10 for Clinical Trials”, describes the BQSI Expert Working Group’s objectives in further detail. To download the white paper and a copy of the guidance document, visit http://info.synomicspharma.com/bqsi/.

Press Contact: Cheri Wilczek, (973) 492-8108

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