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Ask an expert.

Do you have questions about how the FDA Proposed GLP Quality System regulatory changes will impact your business? We’ve got you covered. Just send us a note.
 

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Are you at peace with your quality assurance?

You’re not just looking to gain compliance—you’re protecting your company’s reputation. Let us help you find your inner peace through a compliance update.

 

See how.

What keeps you up at night?

Our clients tell us that it is risk, inefficiency, and poor procedures.

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We help companies manage risk.

Maintaining compliance supports data integrity, quality of processes and timely delivery.
 

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Auditing

Need to know exactly how your current quality assurance systems are performing? Our highly trained auditors can investigate every aspect of your policies and procedures so you know exactly what’s working…and how you can make everything run even more efficiently.

Consulting

Whether you need help with a single compliance project or a company-wide quality service overhaul, QA Compliant will work side-by-side with your team and use proven processes to create a just-right approach for your business.

Training

Knowledge is power, and we believe in giving you the power to control your company’s compliance. QA Compliant can train your current staff about the ins and outs of your industry’s quality systems, giving you a competitive edge.

Computer Systems Validation

Regulated companies (i.e. pharmaceutical, biotechnology, medical device, etc.) are mandated by the FDA, Health Canada, MHRA, EMA and other regulatory bodies to perform Computer Systems Validation. CSV can be complex, time consuming, costly, and risky. We can help.

Industry Best Practices

Are your standards and procedures up to date? Get a consultationChoose your industry

We help make quality possible, and risk nonexistent.

Whether you’re in Pharma, Ag, or Manufacturing, your business is all about consistently providing your clients with a quality products and services.

What a coincidence…at QA Compliant, that’s exactly what we do, too.