We spoke virtually with MilliporeSigma’s head of Process Solutions Andrew Bulpin about his predictions for the CDMO space in 2022.

Millie Nelson, Editor

January 24, 2022

4 Min Read
Continuous processing and CGTs: MilliporeSigma on CDMO trends for 2022
Image: Andrew Bulpin, Head of Process Solutions at MilliporeSigma

BioProcess Insider spoke virtually with MilliporeSigma’s head of Process Solutions Andrew Bulpin about his predictions for the company and the CDMO space in 2022.

The life sciences services division of Merck KGaA, MilliporeSigma, has been steadily increasing its contract development manufacturing organization (CDMO) services through a string of investments and expansions.

The firm invested $110 million into its gene therapy CDMO business in April 2020 by building a second facility at its site in California, adding 11 production suites and more than doubling its viral vector capacity.


Image: Andrew Bulpin, Head of Process Solutions at MilliporeSigma

It accelerated $47 million worth of expansions in December 2020 in Massachusetts and New Hampshire after a surge in demand for bioprocess equipment from Coronavirus therapy and vaccine developers. And most recently, the firm bolstered its messenger RNA (mRNA) offerings through the $780 million acquisition of CDMO Exelead.

Andrew Bulpin (AB): Industry growth and dynamics are contributing to an acceleration in outsourcing efforts, specifically by the success of novel modalities and emerging biotech companies that represent a large portion of the drug pipeline.

BI: Would you describe this as a macro or micro trend?

AB: In their journey to bring their molecules to market, these small companies need expertise in navigating the complex journey to commercialization and are turning to CDMOs to bring drugs to market faster. As such, outsourcing has become a macro trend in itself.

BI: What about in-sourcing?

AB: [There are] some exciting manufacturing trends in ‘in-sourcing,’ as we see the adoption of continuous processing coming into its own while we evolve to BioPharma 4.0. In 2022, we expect to see companies further intensify their unit operations as they continue to eliminate bottlenecks in their process.

BI: Do you have any examples of this happening at MilliporeSigma?

AB: Our work with Transcenta is a nice example of this, as they leverage flow-through polishing purification technology and evaluate additional technologies to enable connected and continuous processing. Process analytical tools that enable real-time testing will also advance the move to continuous processing.

AB: One of the boldest macro trends certainly is the increased advancements for innovative cell and gene therapies and viral vectors, which drive productivity, scale-up and standardization of these therapies.

BI: What path do you expect this trend will take in 2022?

AB: In 2022, we expect to see the effects of those advancements realized, which will allow companies to get into manufacturing much faster. For instance, we made an investment in our Carlsbad, California facility to now support all industry standard virus types (AAV, LV and Retro) all the way up to 1000 L for viral vectors.

BI: Is there anything else you can predict happening in this sector in 2022?

AB: Continuous processing will become a gamechanger as the industry’s focus on increasing its sustainability grows. Smaller facility footprints and reduced utility usage provide an attractive path to carbon neutrality.

BI: How would you describe companies seeking contracting partners?

AB: Our customers are reshaping modern medicine by transforming how diseases are treated. They must navigate through process development, scale-up, manufacturing, commercialization, and regulatory compliance to advance current drug technology and bring new curative treatments to the forefront. Oftentimes, the molecule IS the company, so choosing a CDMO to collaborate with is a very important decision. Transparency is paramount – they want a true partnership with their CDMO, not to be excluded from the decisions and process regarding their molecule. Flexibility is key in helping them meet their critical milestones.

BI: What would you say is the driving force for current demand you are experiencing?

AB: Our adaptable processes, broad product portfolio, global network and technical experts all help our customers reach their critical milestones. Customers also have access to our leading BioReliance testing services.

BI: What makes you different to other CDMOs?

AB: Many CDMO providers offer primarily manufacturing services. Our unique CDMO services integrate contract development, manufacturing, and our leading biosafety testing portfolio with the industry’s broadest product offering – all streamlined with a single, highly experienced provider. Very few companies can provide this breadth of services AND a complete product line. The synergies gained through our work in CDMO help drive our product and template innovation, ensuring they work seamlessly in our processes. We are pioneers in partnership to advance human progress.

About the Author(s)

Millie Nelson

Editor, BioProcess Insider

Journalist covering global biopharmaceutical manufacturing and processing news and host of the Voices of Biotech podcast.

I am currently living and working in London but I grew up in Lincolnshire (UK) and studied in Newcastle (UK).

Got a story? Feel free to email me at [email protected]

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