Webinar recording | Explore the journey of a chromatography project from lab to industrial

Webinar recording 

Duration: 50 minutes

Departure gate: a material to purify

Arrival gate: an efficient industrial process

Each separation features unique characteristics. So how can you derisk your purification process scale up? By developing the separation process through a checkpoint pathway.
This presentation will highlight a step by step approach used to ensure the development of a purification process, starting from laboratory throughout the whole life cycle of the industrial equipment. An example of process development will be presented: the high purity fructose syrup production.

Objectives: Minimize risk, save development time, maximize cost efficiency

Why you should attend this webinar?

In this webinar, you will learn what to check at each step of purification process scale up, illustrated by the example of a high purity sugars product: the high fructose syrup (HFS) at 98% purity. 

The step by step approach can be explained in 8 steps:

1. The project brief with the definition of feed material
2. The lab screening of the resin
3. The in-house numerical process simulation
4. The first process evaluation
5. The pilot scale validation
6. The process design
7. Engineering
8. Commissioning

By following this approach we better control development time and so participate to shorten time to market. Besides, with a proper R&D and process development working closely together, the cost efficiency of the process is maximized.

Speakers:

Alexandra Gimbernat, PhD, Product Manager, Novasep Process Solutions Alexandra Gimbernat joined Novasep in 2018 with a chemical engineering degree and a background in sugars through her PhD on sugar catalysis and separation process. She starts to work as part of the Research and Development team and now she works as Product Manager at Novasep Process Solutions.

Hector Osuna-Sanchez, PhD, R&D Manager, Novasep Process Solutions Hector Osuna-Sanchez is a chemical engineer and PhD with expertise in chromatographic processes for pharma, biopharma and industrial biotech. He joined Novasep in 2020 as R&D and Pilot Manager, heading a 10-people team with lab and pilot capabilities coupled with numerical tools for efficient development and scale-up of purification industrial processes.

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