Quality assurance and regulatory compliance services for
pharmaceutical and biomedical research and development
BioResearch Monitors, Inc.
Established in 1992 provides professional, cost-effective quality auditing, and consulting services related to FDA, ICH, ISO and related worldwide quality standards for good clinical practices (GCP), good manufacturing practices (GMP), good laboratory practices (GLP) and related quality standards for pharmaceutical research and development.
BioResearch Monitors, Inc. is a consulting group specializing in Quality Assurance and Regulatory Compliance assessments of Pharmaceutical and related Biomedical Research and Development activities. Gary T Sniffen, the President of BioResearch Monitors, Inc. has been involved in managing, conducting and establishing standards for Worldwide Research Quality Assurance since 1981. Our Quality Assurance and Clinical Research Associates are all highly qualified professionals with significant industry, medical and/or government (FDA) experience.
BioResearch Monitors, Inc. conducts audits and evaluations which assess the quality and integrity of research data; evaluate compliance with U.S. and multi-national regulatory obligations pertaining to Sponsors, Monitors, Clinical Investigators & Institutional Review Boards; and document that studies were audited by an independent Quality Assurance group.