Services

Services

As a global leading CDMO, we support your process development and manufacturing needs for biopharmaceuticals. We also support you with the creation of approval documents at an international level. Many years of experience and expertise in finding best-fit solutions, as well as certified quality management and advanced technologies, ensure our high-quality standards. Furthermore, our client-oriented consulting activities, including project management and regulatory support, guarantee your project’s success.

With our full-service offering, we are your CDMO partner of choice.

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Bioprocess Development

Stability from the beginning

We develop stable and robust cell lines and establish cell banks (MCB and WCB). We also develop and optimize processes for the manufacturing and purification of recombinant proteins. Our world-class analytical capabilities and best-in-class formulation development in collaboration with Leukocare complete our portfolio.

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Manufacturing

Quality at every scale

Our drug substance manufacturing in state-of-the-art cGMP facilities meets the highest standards of the biopharmaceutical industry. Each manufacturing process is scalable for different requirements - for clinical trials as well as for market supply.

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Associated Consulting Activities

Reaching our goals together

With our active commitment and professional advice, every project with Rentschler Biopharma is in expert hands. Our experience in approval strategies at an international level ensures that your product is documented in accordance with regulatory requirements.

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Cell and Gene Therapy

Rentschler ATMP Ltd.

Rentschler Biopharma is your trusted CDMO of choice, ready to advance your cell and gene therapy development. You need a partner with a strategic approach, ability to scale-up and get your product to market quickly? With our history of excellence, we have a deep understanding of manufacturing processes and process development, always adhering to our uncompromising quality standards. We treat your project as if it were our own, applying our unmatched knowledge in biopharmaceutical production and CMC requirements.

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