Find a GxP Auditor & Regulatory Expert
Independent Auditors, QMS Consultants, Regulatory Strategists, and More
Discover qualified independent consultants and subject matter experts across pharmaceuticals, biotechnology, and medical devices. Find specialized support for mock inspections, gap assessments, validation, supplier audits, regulatory remediation, and all other needs.
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Regulatory Affairs & Compliance
FDA Regulatory Compliance and QMS Expert with 10+ years of experience and 100+ conducted GMP/GSDP audits. Specializing in FDA 21 CFR, EU GMP, mock inspections, risk management (ICH Q9), and ISO 13485 compliance.
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Quality & Validation
Pharmaceutical Quality Assurance and In-Process QA (IPQA) specialist with expertise in Good Manufacturing Practices (GMP) documentation, Batch Manufacturing Record (BMR/BPR) review, line clearance verification, and compliance data management.
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Software & Digital
Top-Rated Manual QA Engineer with 8+ years of experience and 475+ completed engagements. Specializing in functional testing, mobile and web verification, API testing, and defect management.
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Software & Digital
Specializing in SaaS, Web, and AI-enabled platforms with 120+ verified technical engagements and a 100% success rate. Expert in manual and automated defect discovery, API verification, and test lifecycle execution.
Need Specialized Guidance or a Custom Audit Team?
If you have specific audit scopes, urgent FDA inspection remediation needs, or require a specialized team of regulatory experts, reach out directly to our coordination team at info@gxpsource.com.