2000-present (23 years)
Diane Gleinser
Vice President, Life Science Services & Solutions at USDM Life Sciences
Diane Gleinser Email & Phone number
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d***@usdm.com
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Diane Gleinser Work Experience Summary
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4Average duration at a company (years)
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4Last Update 4/7/2024 9:23 PM
About Diane Gleinser
Diane has over three decades of experience in the life sciences industry and leads a highly skilled team of implementation and compliance engineers. Her in-depth knowledge of the regulatory landscape and unwavering passion has been instrumental in rooting USDM's focus on regulatory compliance for life sciences customers. Over her tenure, Diane has mastered quality assurance, quality control, validation and regulatory compliance for R&D, clinical affairs, manufacturing and packaging, laboratory setup and analysis, and auditing under cGMP, cGLP and cGCP regulations and 21 CFR Part 11. She holds a B.S. in Biology from San Diego State University and a Certification in Pharmaceutical and Medical Device Law from Seton Hall University.Read moreDiane Gleinser Current Workplace
Diane Gleinser Work Experience & Education
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Update from FDA on CSV Changes
Diane Gleinser : Today, we'll be talking about why the FDA is moving from validation to assurance and what that means. Diane Gleinser : While we're a...Getting Results on Regulated Projects with Virtual Teams
Vice President of Life Sciences Solutions Diane has more than 29 years of experience in the life sciences industries. As a member of the senior manag...USDM Leadership Team | Life Sciences Regulatory Compliance
Diane Gleinser Diane Gleinser Vice President of Life Science SolutionsJun 25, 2021
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Diane has over three decades of experience in the life sciences industry and leads a highly skilled team of implementation and compliance engineers. Her in-depth knowledge of the regulatory landscape and unwavering passion has been instrumental in rooting USDM's focus on regulatory compliance for life sciences customers. Over her tenure, Diane has... mastered quality assurance, quality control, validation and regulatory compliance for R&D, clinical affairs, manufacturing and packaging, laboratory setup and analysis, and auditing under cGMP, cGLP and cGCP regulations and 21 CFR Part 11. She holds a B.S. in Biology from San Diego State University and a Certification in Pharmaceutical and Medical Device Law from Seton Hall University.Read More