Your Challenges Require Smart Solutions:
PharmaABF - Clinical Trial Supply QP Release

QP Release

The expertise to guide

At ABF we have the expertise to guide your product all the way to QP release.

EU Batch Certification

EU Batch Certification

Whether for commercial sale or clinical trial use, a finished product must be certified and released by a Qualified Person (QP). This process is known as a QP release.

Delivery to customers takes place only after our QP has released every batch produced and controlled in accordance with the relevant country’s legal requirements.

The experience of our Qualified Person ensures that we swiftly and expertly handle specific issues across the pharmaceutical spectrum – from small molecules to biopharmaceuticals and Advanced Therapeutic Medicinal Products (ATMPs).

Our Range of QP Services include:

  • QP Back-Up Services
  • Advice Relating to Regulatory Requirements
  • Assistance with Batch Expiry Extensions
  • Issue of QP Declarations and Manufacturing Site Audits
  • QP Release Certification and Batch Release
  • QP Batch Release and Consultancy Services for ATMPs
  • Consultancy Services regarding GMP, GCP, GDP and GLP

Your direct contact

Benjamin Baranyai
Senior Business Development Manager
+43 676 897 11 55 20

Business Development

Contact us!

To learn more about us and what we can do for you please contact our Senior Business Development Manager

Contact form


Do you have any questions about our service?

Contact form

Our experienced and committed team offers a comprehensive range of services in the following areas

Labeling & Packaging



Import & Export

Quality Management



Clinical Trial Supply

GBA Group Pharma

Stay in touch

GBA Group Pharma Newsletter

Always stay up to date and register for our newsletter.

© 2020 GBA Group
Data PrivacyLegal NoticeTerms & ConditionsDisclosure