Comprehensive Pharmaceutical Validation Services

Compressed timeline leading to production variance and poor product quality? 

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

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

Talk to a validation expert.

Validation Services that Turn Compressed Timelines Into Compliant Ones

From fully managed, continuous CQV (commissioning, qualification, and validation) to on-demand services for process validation, packaging validation, software assurance and more, we simplify workflow complexity—assessing risks, closing gaps, and ensuring compliance at every turn. All while meeting your aggressive timeline and budget constraints.

CQV

CQV (Commissioning, Qualifications and Validation)

Ensure your systems, equipment, and processes meet stringent regulatory requirements and quality standards so you can produce high-quality pharmaceutical products.

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Building Commissioning

Avoid costly inefficiencies, reduce operational risks, and ensure your building systems perform as intended with a thorough commissioning process.

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 optimal cleanroom performance with precise airflow visualization.

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CSV (Computer System Validation)

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

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CSA (Computer Software Assurance)

Safeguard data, optimize performance, and mitigate threats with CSA measures made to ensure compliance now and in the future.

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PPAP (Production Part Approval Process)

Align components, materials, and manufacturing methods with quality standards with robust PPAP services made to improve efficiency and accelerate time to market.

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Digital
Validation

Simplify and accelerate your validation process with industry-leading digital platforms and expert-led services.

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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.

LET'S TALK