Staff Members With Expertise In
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John R. Godshalk MSE, MBA

CV

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Phone: 703-485-6139

Expertise in cGMP compliance, facility design and regulatory requirements, quality assurance, audits/inspections

Eugene B. Johnston CQE, CQA

CV

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Phone: 919-657-0435

Expertise in quality management and regulatory compliance

Ronald A. Marchesani

CV

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Phone: 650-378-1303

Expertise in compliance audits, facility design evaluation and quality system development/evaluation/oversight for biotechnology products

Jim McIver Ph.D.

CV

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Phone: 781-718-5734

Expertise in product management, development, manufacture, control and regulatory submission for biological products and bioassays

Andra E. Miller Ph.D.

CV

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Phone: 301-320-9537

Expertise in CMC, regulatory and GMP requirements for cell and gene therapy products

Reginald D. Neal

CV

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Phone: 202-294-8543

Expertise in facility inspections, facility validation and regulatory requirements

Peter Probst

CV

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Phone: 301-831-3007

Expertise in GMP compliance; quality assurance; facility audits/inspections, facility validation & regulatory requirements; facility design evaluation

Nadine M. Ritter Ph.D.

CV

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Phone: 240-372-4898

Expertise in analytical CMC technical and regulatory requirements and R&D/GLP/GMP laboratory quality practices for biotechnology products

Darin J. Weber Ph.D.

CV

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Phone: 206-940-3923

Expertise in regulatory strategy and CMC development for cell-based therapies and engineered tissues

Larry K. Winberry Ph.D.

CV

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Phone: 248-396-5818

Expertise in quality systems, manufacture and control, and product development for biological products

David Rouse M.S.

CV

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Phone: 919-303-1624

Expertise in research, review and regulation of biological products within CBER and the biopharm industry.

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