Future-Proof Your CDMO

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Learn How to Use Data Analytics To Improve Processes and Generate Revenue for your CDMO

Growing competition and the trend toward digitalization in the biopharma industry means that in order to keep up, you need to leverage your CDMO's most important asset: data.

Leveraging your data can help you realize:

  • Quality and Regulatory Assurance through enhanced process understanding and control
  • Increased Partner Trust through increased external collaboration and process transparency
  • Maximized Revenue through COGs optimization and accelerated delivery times

 

Watch this recent webinar to uncover a competitive advantage

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How Can CDMOs Unlock the Value of Data?

Data is the new oil. However, just like oil, data needs to be refined and properly put to work. Sartorius Data Analytics is the leading provider of advanced data analytics solutions to the biopharmaceutical industry. Our data refinement offerings include MODDE®, for design of experiments, SIMCA® for multivariate data analysis, and SIMCA®-online for real-time process monitoring.

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Book a Free Strategy Session to Learn More

Achieving profitability, growth and staying ahead of competitors means leveraging one of your most important assets: data. As the CDMO market consolidates and becomes more competitive, those who tap into the real value of data can use it to gain recognition as strategic differentiators, provide market leadership, and ultimately become more profitable.

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You will learn:

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How to leverage your data  to secure long-time strategic partnerships

 

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How data can be used to maximize profitability

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How data can be used to speed up timelines and accelerate delivery

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Customer Case Story

In this publication, FUJIFILM discusses how SIMCA® and SIMCA®-online can be leveraged to accelerate chromatography review for faster and more reliable operations. FUJIFILM Diosynth Biotechnologies also uses SIMCA®-online as a portal for their customers to have full transparency into their processes.

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Piramal

Poster

Use of Design of Experiments to Define Manufacturing Process Conditions for an ADC

This poster by Piramal Pharma Solutions describes the use of MODDE® Design of Experiments to determine robust setpoints for the reactive stages of an Antibody-Drug Conjugate (ADC) process.

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Development of an ADC Process with Single-Use Membrane Technology

This poster by Abzena shows how MODDE® Design of Experiments can be used to optimize membrane chromatography screening and scale-up for an Antibody Drug Conjugate (ADC) process.

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Read More From Our Blog

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How CDMOs Can Use Data Analytics as a New Source of Revenue

The global biologics market is one of the fastest growing segments of the pharmaceutical industry. But development and production can’t keep pace with discovery. That’s one reason outsourcing to contract development and manufacturing organizations (CDMOs) continues to increase. 

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How Data Integrity Helps CDMOs Attract Partners

In spite of the increasing level of importance regulatory agencies place on data integrity and security, many small and large CDMOs don’t have the right systems in place to manage their data properly. How can CDMOs move to the next level and digitalized their data management and processes? 

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How CDMOs Can Implement a Modular PAT Strategy

Process analytical technology (PAT) is playing an increasingly important role in the pharmaceutical and biopharmaceutical industries due to regulatory pressure and the push to reduce costs while managing quality. For CDMOs, any investments into PAT technology must be versatile enough to accommodate a variety of products and processes.

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Trending Technologies that Accelerate Process Development for CDMOs

Trending Technologies that Accelerate Process Development for CDMOs

Adopting a strategy that facilitates rapid and reliable development and scale-up of bioprocesses is an urgently growing priority for contract development and manufacturing organizations (CDMOs). The most successful CDMOs have identified strategies for completing projects efficiently and effectively while incorporating QbD approaches.

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Watch a Webinar

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How Data Analytics can Boost the Bottom Line at a CDMO

By innovating their service offerings, CDMOs can address some of the major challenges their partners face when deciding to outsource their operations, like loss of control or quality management. In this webinar, we will propose a scenario in which a CDMO can double the return on investment in just one year! 

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OSIsoft and Sartorius Partner to Help CDMOs Leverage their Data

Learn how contract pharma organizations can gain additional insights from their data to become more profitable and increase partner trust. Hear a success story from FUJIFILM Diosynth Biotechnologies, which paired the OSIsoft PI System with advanced data analytics tools to achieve a tenfold optimization in resource expenditure.

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How CDMOs can Adopt a Modular PAT Strategy

When CDMOs investigate the use of PAT they must be assured their ROI, therefore the PAT technology they invest in should be versatile and modular – working with a range of processes and modalities. The Sartorius BioPAT® Spectro Raman tool gives CDMOs working in a high-paced environment the opportunity to unlock the full potential of Raman spectroscopy.

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Putting the “D” in CDMO with Data Analytics and Ambr®

Biopharmaceutical companies have placed an increased reliance on contract development and manufacturing organizations (CDMOs) for all aspects of process development. However, as a CDMO, how can ensure that you’ll be able to meet the aggressive timeline expectations set out by your clients? In this webinar, Sartorius experts will discuss how to accelerate process development timelines. 

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How CDMOs Can Digitalize their Cell and Gene Therapy Processes

One of the most important considerations for companies working in the CGT (cell and gene therapy) field is how to ensure commercial success of the product. By developing a strong relationship with the right CDMO, CGT developers can chart out a development, scale-up, and manufacturing plan that aligns with both their clinical and financial needs.

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Application of DOE (Design of Experiments) to Antibody Drug Conjugates (ADC) Process Development

Find out the Piramal approach to the development of Antibody Drug Conjugates processes. Specifically, it will focus on the use of DOE to develop the key reactive stage of a standard ADC process. The impact of process parameters on product quality attribute, namely Drug-to-Antibody ratio was assessed via full factorial design. The analysis of the design was assessed via Sartorius MODDE® 13 software. The software enabled to modelise the effects of parameters, allowing identification of set points for safe upscaling of the process.

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