Our Services
At Verity, we provide expert consulting services that bridge scientific innovation with regulatory excellence. With over two decades of experience in biotech, pharmaceuticals, and life sciences, we offer comprehensive support across quality systems, compliance, validation, laboratory setup, and scientific development. From startups to established teams, we help you move forward with clarity, confidence, and compliance.
Contact our expert team for a free Consultation & see how we can support your success.
Quality Systems & Compliance
• Quality Management System (QMS) design and optimization
• Regulatory compliance support (FDA, GMP, GLP, CLIA, GxP, 21 CFR Part 11)
• CAPA development and root cause analysis
• Internal audits and inspection readiness
• Quality Assurance (QA) and Quality Control (QC) advisory
Documentation & Technical Writing
• SOP writing and lifecycle management
• Regulatory documentation and validation reports
• Scientific writing and technical editing
• Document audits and compliance alignment
• Instrument validation and qualification (IQ/OQ/PQ)
• Method and assay development & validation
• Technology onboarding and method transfer
• Lab setup and infrastructure planning
• Lab troubleshooting and operational efficiency
Validation & Laboratory Support
Scientific Consulting & Experimental Design
• R&D strategy and protocol development
• Custom experimental design for biologics, molecular studies, and validation
• Troubleshooting experimental workflows
• Scientific advisory and data interpretation
Training, Documentation & Startup Support
• GxP and SOP staff training (non-certification)
• Onboarding support for lab and QA/QC teams
• QMS and SOP infrastructure for startups
• Interim QA leadership and quality coaching
Contact us
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