• Compliance: Full Audit Readiness with 70% Less Personnel Work

Laboratory products

Compliance: Full Audit Readiness with 70% Less Personnel Work

Assuring time- and cost-efficient compliance and traceability - crucial to delivery of safe, high-quality products - is a challenge in the tightly regulated pharmaceutical and biopharmaceutical industries.

Anton Paar’s ViscoQC 300 turnkey customised qualification package, along with qualified installation support, delivers a fully qualified analytical environment and reduces in-house personnel work by 60% to 70%. The qualification goes significantly beyond simple installation and basic IQ/OQ. It involves individual preparation for every system. A detailed risk analysis, performance qualification, traceability matrix, and final qualification report increase the value of the qualification package for the whole qualification process for the customer.

Looking for advanced data integrity and 21 CFR Part 11 compliance? With the V-Comply software, which also includes the Pharma Qualification Package, you cover all necessary requirements like audit trails, electronic signature, data security, login controls, user authentication, and many more - all of which can also be proven during qualification.

Additionally, each Anton Paar qualification package comes with a customisable SOP template as a base for the customer’s own SOP. The documents used can be fully and seamlessly integrated into the user’s own qualification process and comply with

Thousands of customers trust Anton Paar's expertise. Thousands of qualified instruments have passed audits with Anton Paar qualification documents.

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