BioTech/Drugs - N/A, N/A, US
Quality Auditing, and Quality Management Systems Development in the Human Tissue for Transplantation Industry.Specializing in compliance issues for Current Good Tissue Practice Regulations (21 CFR 1271); Medical Device (21 CFR 820); Non-clinical GLP Laboratories (21 CFR Part 58); ISO 9001:2008 and ISO 13485:2003 Quality Management Systems Requirements
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