Consistent, reliable audits,
We’re people turning compliance into meaningful value worldwide.
The audit standards you need, executed by experts
A system to ensure and control that products are being elaborated under the appropriate quality standards.
Service providers for the storage and transport of goods will have to comply with different regulations.
Assessment of compliance with the minimum requirements of any clinical trial or clinical quality management plan.
Every laboratory research and development action/initiative needs to be carried out under specific conditions.
Analysis of computer-supported systems in the pharmaceutical industry to assess whether they follow the stipulated set of guidelines that maintain their operational efficiency and reliability.
Any organization wishing to hold a marketing authorisation for a medicinal product must comply with a number of quality standards relating to its organization and operation.
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Qualifyze in numbers
Happy Qualifyze customers
Total audits conducted
Auditors in our network
Countries where we’ve audited
Meet some of our quality experts
Melina Lozano Vigil
Quality System Officer
Biomedical Scientist. Dedicated and determined to improving quality, safety and sustainability since 2018.
Chemist passionate about GMP guidelines. Extensive experience in auditing with a focus on API and Excipient audits since 2015.
Medicinal chemist. Experience in compliance consulting services (CQV, Data Integrity, Inspection Readiness). Passionate about pharmaceutical technology and supply chain solutions.
Head of Quality
Pharma-Biological Chemist. Committed to Quality and collaboration for finding solutions. Involved in GxP audits since 2015.
VP of quality
Pharmacist captivated with supplier qualification since 2015. Quality oversight is my motto.
We’ve helped more than 659 companies stay compliant.
Why we’re trusted by some of the biggest names in pharma.
Feel supported by our team of audit experts with decades of combined experience. Let people you trust take the entire audit burden off your plate.
Centralized audit management
Centralize all audit-related communications including CAPA follow ups, document signings, invoicing and more. All in one secure, digital platform.
Audit reports, made simple
Expertly designed to deliver you information in a crisp, clear format. Impeccable english and traffic light CAPA follow up system for an easy, actionable review process.
We can facilitate better communication with auditees, more flexible audits and less C02 emissions thanks to our large network of international, multi-lingual auditors.
Standardized and consistent. Audit reports, the Qualifyze way.
Our audit reports have been designed with your (precious) time in mind. Simple to skim and delivered in a consistent format, every single time.
A data-driven audit management platform, built for your peace of mind
Centralize each and every step of your audit process. Browse audits, sign documents, review CAPAs, approve reports and more, all in one place. Auditing, made easy.
We chose Qualifyze because of their reliable customer service and the good quality of the audit reports at a fair price. Our requests were handled with flexibility and willingness to compromise.
Qualifyze helped us reduce costs and time thanks to their team of experienced auditors.
As promised, our required GMP audit report was delivered by Qualifyze very quickly and met our expectations and needs in terms of quality and time.
When Qualifyze audited us in 2021, we were impressed by the auditor's qualification, precision, and profound knowledge. The audit also helped us a lot since it was comparable to an authority audit.