The Verity Collective offers unmatched depth in quality support across the life sciences industry. Our team of over 500 Subject Matter Experts (SMEs) has built, led, and optimized quality systems at every stage—from early development to post-market. With hands-on experience in global regulatory environments, our professionals ensure that quality processes are not only compliant but also scalable and efficient. Whether you’re establishing a QMS, managing deviations, or preparing for inspections, Verity brings the strategic insight and operational know-how to elevate your quality function.
Quality that Scales You
Quality isn’t just about ticking boxes—it’s about building systems that evolve with your organization. Verity’s network of experts has designed and managed quality programs for startups, global enterprises, and everything in between. From QMS implementation and remediation to deviation management and inspection readiness, we provide practical solutions that align with your stage of growth.
We know no two companies are the same. That’s why we tailor every engagement—whether you need strategic oversight, hands-on execution, or something in between. Our flexible model ensures you get the right support, exactly when you need it.
Quality Operations
Quality Operations
Quality Assurance and Quality Control
CMO/CDMO Oversight
Batch Record Review
QC Stability Program
Data Review
Method/Process Development
API/Cell Therapy/Gene Therapy
Tech Transfer
Inspection Readiness
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Quality Systems & Compliance
Quality Systems & Compliance
Quality Management Systems (QMS)
Process and Procedure Development
Electronic Systems (eQMS)
CAPA/Deviation/Change Control
Quality Investigations
Risk Assessment
Implementations
Remediations
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Auditing
Auditing
Good Manufacturing Practice (GMP)
Good Clinical Practice (GCP)
Good Laboratory Practice (GLP)
Good Documentation Practice (GDP)
Good Pharmacovigilance Practice (GVP)
Bioresearch Monitoring (BIMO)
Mock Pre-Approval Inspection (PAI)
EX-FDA
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