Novasep Process : Pharmaceutical Business Unit Products and Services

Novasep Process is a world leader in preparative and process chromatography and is able to offer both chromatography units and chromatography services for the purification of pharmaceuticals.

For any request regarding chromatographic separation, please contact us.

Purification and Separation Systems

Novasep Process designs and supplies preparative chromatography systems, for the purification/separation of pharmaceutical compounds, ranging from lab-scale to industrial and production scale. Our scope integrates solvent recycling and storage units.

Modelling Software

Novasep's process modelling software and numerical tools are developed in-house to model and optimise the design of our chromatographic processes.

Process Development

Novasep's purification process development services include screening, feasibility studies, optimization, as well as process scale-up and validation.

Custom Purification

Novasep Custom purification services involve purification of pre-clinical and phase I through III products, process validation and separation / purification of commercial intermediates and APIs, in its FDA inspected facilities.

Chiral Stationary Phases (CSP)

Novasep Process can propose a full production process including a chromatographic system together with appropriate CSP (Chiral Stationary Phase).
For best results, Novasep Process signed a strategic technical co-operation alliance with Daicel and Chiral Technologies.

Pharmaceutical Development and Production

Novasep Process is also involved the development and production of pharmaceuticals with specialized technologies and know-how.

It specialises in:

• Preparative and process chromatography
• Evaporation / distillation / solvents recycling
• Crystallization
• Control of the solid chain - particle size, and polymorphism (APIs)
• Global process design / integration

For any request regarding chromatographic separation, please contact us.

Benefits and Advantages

Time

Novasep's chemists and engineers quickly design the right chromatographic separation method for your molecules with Chromatographic technologies and systems such as HPLC, Cyclojet, Continuous Chromatography, SFC. We will run or deliver systems for you to bring your pure API to clinical trial in reduced time.

Cost

To meet your cost objectives, we will develop and validate the right chromatographic process that will provide you the best productivity and return on investment.

Freedom

Feel free to ask for more: we are able to combine multi-step synthesis and chromatography in one of our six FDA-inspected sites. To in-source or out-source your production, we will provide the purification system at your required scale and transfer the process to you.

Other

Please challenge us!

Contact: pharma@novasep.com