Shared audits are planned audits that combine multiple customer requests into one audit. When we combine multiple customers into one audit, we can execute various “audits” simultaneously. We do this by extending the audit scope, meaning more products are audited in one audit. That means instead of trying to execute multiple audits across multiple days, we can save the auditees time and resources by rolling them all into one audit event.

Recently published audit reports executed by us on behalf of one or multiple clients. These audit reports are active and ready to purchase directly from our platform, making them ideal for customers with last-minute audit needs. It’s our most efficient and cost-effective audit service. With hundreds of audit reports in our database, we likely have the existing audit report you’re looking for.

GAMP (Software), GCP (Clinical), GDP (Distribution), GLP (Pre-clinical testing laboratory), GMP (API), GMP (Excipients), GMP (Finished dosages), GMP (Packaging), GMP (Medical device), GMP (Subcontracted laboratory), GMP (Starting materials), GVP (Pharmacovigilance), ISO 9001 and ESG.

No, you must give us written permission for every report we sell to additional customers who were not part of the original audit. We will never share any information without your express consent. Transparency with our stakeholders is one of our core values.

We will only display your name, the site’s location, audit standard, and audit date. All other information will only be available to the customer after you have approved their admission to the audit.

Yes, all our customers agree to our confidentiality terms and conditions when we sign the contract. If required from your side, we can also facilitate a 2-way or 3-way CDA signature process.

No, Qualifyze will never charge you for our service. We will always remain independent, but a scope extension benefits all parties.

We always try to respect the previously agreed audit time frame. This depends, however, on how many additional products will be audited. If need be, we may need to consider a different audit date.

By using a systematic approach, meaning we audit one product from every workshop. Those products can then be used as an exemplary product and allow us to include other products manufactured under the same QMS and in the same workshop.