The Verity Collective offers unmatched depth in quality support across the life sciences industry. Our team, with a seasoned network of 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
We support your quality operations by managing oversight, reviewing data and batch records, and ensuring your processes, methods, and partners are ready for tech transfer and inspections.
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- 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
Quality Systems & Compliance
Effective quality systems start with clear processes, strong compliance practices, and the right tools. From QMS development and eQMS implementation to investigations, change control, and remediation, our team ensures every element supports long-term success.
- Quality Management Systems (QMS)
- Process and Procedure
- Development
Electronic Systems (eQMS) - CAPA/Deviation/Change Control
- Quality Investigations
- Risk Assessment
- Implementations
- Remediations
