Comprehensive Pharmaceutical Packaging Validation Services

Compressed timeline leading to production variance and poor product quality?

Performance Validation is here to solve your pharmaceutical packaging challenges. Our team of experts ensures your entire pharmaceutical packaging workflow meets stringent regulatory requirements and cGMP quality standards.

Ready to simplify packaging validation? Fill out the form to talk to one of our pharmaceutical experts.

Talk to a packaging validation expert.

Validation Services that Turn Compressed Timelines Into Compliant Ones

Our pharmaceutical packaging validation services are grounded in cGMP compliance. Whether you’re launching a new drug package, qualifying cold-chain transport, or documenting packaging system performance, we can help you save time while demonstrating regulatory compliance.

CQV

CQV (Commissioning, Qualifications and Validation)

Ensure your systems, equipment, and processes meet stringent regulatory requirements and quality standards across every packaging line, cold room, and transport unit.

TempMapping

Temperature
Mapping

Maintain consistent and compliant temperature conditions and safeguard product quality with comprehensive mapping services tailored to your facility.

CAV

CAV (Critical Airflow Visualization)

Reduce contamination, identify hazards, and ensure clean and controlled packaging operations with detailed airflow visualization.

cq-testing-boxed

CSV (Computer System Validation)

Verify the integrity, reliability, and compliance of computer systems with CSV services that optimize system performance.

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Creating Better GMP Manufacturing Workflows

PV has decades of experience qualifying and validating Pilot, Active Pharmaceutical Ingredients (API), and final production lines for small and large molecules and vaccines using batch and continuous manufacturing processes. With PV’s expertise, you can identify any potential risks or issues in your workflow before they become significant concerns. Our proactive approach helps you minimize downtime and ensure that production stays on schedule, saving time and resources.

Why Performance Validation?

Performance Validation (PV) is a global validation partner for pharmaceutical and medical device manufacturers. Headquartered in Indianapolis, IN, we specialize in turning compressed timelines into compliant ones using innovative, adaptive approaches that balance production realities with strict regulatory requirements. Our best-in-class, cGMP-compliant services cover diverse needs, from fully managed CQV to on-demand temperature mapping, smoke studies, software assurance, and more. With a dedicated team consisting of more than 95% engineers, we work closely with regulators and equipment suppliers to keep validation ahead of production curves and keep quality moving forward.

37

Years in Business

130

Full Time Validation Experts

300 +

Clients Served

20 k+

Total Projects

Your Validation Partner for What’s Next

For over 30 years, PV has helped countless pharmaceutical clients with validation services. Find out how our experts can help your company improve product quality and compliance, while becoming more efficient.

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