Batch Release, Supporting Analytical Studies and Services

Utilize our procedures to gather quality data and perform comparative analysis to ensure every cGMP batch manufactured by us is QC tested and released according to product specifications.



With you on your biologics journey...

Why batch release?

Qualified Persons (QP) are responsible for ensuring that each product batch is manufactured according to the relevant laws, Marketing Authorization (MA) requirements, and compliance with cGMP guidelines.

3P´s batch release, supporting analytical studies and services

Comparability studies

Products that have changed in the original manufacturing process are subject to additional comparability studies, ensuring that no changes have been made impacting quality, safety, and efficacy. To support these requirements, our experts gather quality data before and after the modifications and perform a comparative analysis of all available information to confirm that any changes have no adverse effects on the physicochemical or biological attributes of the final product.

Stability studies

Drug Substance, product intermediates (if applicable) and Drug Products are subject to stability studies, allowing us to assess sensitivity to factors that may impact the product’s activity, safety, and quality. Before performing stability studies, we prepare a stability protocol reflecting the actions and conditions used for study execution under long term, accelerated and stress conditions.

Fill and finish

Our solution-driven approach to support you throughout your biologics journey ensures that all Fill and Finish activities are managed in-house according to the specifications on format, fill volume and final formulation as defined.

Batch release

Every cGMP batch manufactured by us is tested by QC and released according to product specifications before release.

What we will deliver

We ensure all clinical batches, Drug Substance or Drug Product manufactured are safe for intended use by delivering a final GMP compliance certificate and batch release in line with the mutually agreed Quality Agreement and Dossier.

Our dedicated team of specialists will be happy to discuss any of your Batch Release, Supporting Analytical Studies And Services needs. Contact us on +34 948 346 480 or email businessdevelopment@3pbio.com

  • It’s about our capacity and how we visualize and invest in the processes it takes to grow with you. An infrastructure built on an unmatched and shared commitment to ensuring your biologics journey makes a difference to those who need it.

  • It’s about our capacity and how we visualize and invest in the processes it takes to grow with you. An infrastructure built on an unmatched and shared commitment to ensuring your biologics journey makes a difference to those who need it.

  • It’s about our capacity and how we visualize and invest in the processes it takes to grow with you. An infrastructure built on an unmatched and shared commitment to ensuring your biologics journey makes a difference to those who need it.

Get in touch

Let’s discuss your biologics journey.

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