FDA regulatory experts on Good Laboratory Practice and Good Manufacturing Practice, including all aspects of quality assurance and control in the manufacturing process.
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Selected GLP / GMP Experts
- Technical Consultant #1941 - Synthetic Drug Product Development Expert - Marketing and IP Management Resume
- Technical Consultant #1679 - Certified Quality Auditor: FDA-QSR Systems Consultant, Software Quality Analyst and Course Development and Assessment Resume
- Technical Consultant #1875 - Small Molecule Drug Development and Manufacturing Expert Resume
- Technical Consultant #1026 - Pharmaceutical Consultant: Analytical Methods Validation, Computer Systems Validation and QA/QC Resume
- Technical Consultant #2081 - Pharmaceutical Consultant: Drug Development, Regulatory Affairs, Quality, cGMP, FDA, and Clinical Research Resume
- Technical Consultant #2366 - Senior Pharmaceutical Regulatory (FDA, CDER, CBER, CVM) Compliance Consultant Resume
- Technical Consultant #886 - Pharmaceutical and Medical Device Consultant; Blood and Plasma Processing Resume
- Technical Consultant #1207 - Chemical Engineer Specializing In Pharmaceutical Capital Projects and Facilities With cGMP, FDA and ISO Requirements Resume
- Technical Consultant #2228 - Pharmaceutical , Medical Device, Cosmetic, Food Regulatory Compliance Expert Resume
- Technical Consultant #2507 - Radiopharmaceutical Consultant Specific To: QA, QC, GMP, GMP internal Audits, Health Canada GMP Inspections and Expert Resume
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