Be confident that your disinfectants, cleaners, and processes perform as required. Our GMP- and GLP-aligned testing programs deliver the validation data and documentation needed to protect your facility and reputation, including
Strengthen your contamination control programs as standards evolve. Veltek’s consulting teams work alongside your organization to design, validate, and sustain compliant, reliable operations, including
We connect every part of contamination control into one seamless ecosystem—products, validation, documentation, and expertise designed to accelerate compliance and maintain it over time.
From the chemicals that clean your cleanroom to the data that defends your audit, every solution is built to make your process stronger and your workday simpler.
Cleanroom challenges vary by industry, but the need for reliable contamination control remains constant. We support teams across regulated and precision-driven industries, helping each one meet its unique compliance, safety, and quality goals.
Up-to-date safety data and regulatory details to support safe handling and audit readiness.
Batch-specific documentation verifying quality, sterility, and compliance for every product run.
Transparent records of product and process updates to support GMP compliance and inspections.
Cleanroom training materials that help teams standardize procedures and strengthen compliance.
Step-by-step demos showing proper use, application, and best practices for VAI technologies.
For more than four decades, cleanroom teams have relied on Veltek Associates, Inc. (VAI®) to strengthen contamination control. From the first sterile garments to today’s patented disinfection and documentation systems, every advancement we’ve developed helps customers improve consistency, reduce uncertainty, and maintain continuity across GMP environments.