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Workshop on CONTINUOUS CHROMATOGRAPHY FOR THERAPEUTICS 6th 10th September 2015 Swiss Federal Institute of Technology ETH, Rich, Switzerland Course Director: Prof. Massimo Morbidly Equipment sponsor:
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How to fill out continuous chromatography for bioformrapeutics:

01
Prepare the chromatography column: Clean and sterilize the column according to standard operating procedures. Ensure that the column is in good condition and properly equilibrated.
02
Prepare the sample: Isolate the bioformrapeutics sample from the biological source and purify it using standard techniques. Concentrate the sample to an appropriate volume and adjust the pH and conductivity as necessary.
03
Load the sample: Connect the prepared chromatography column to the chromatography system and ensure that the flow rate is set correctly. Load the prepared sample onto the column using the desired loading strategy (e.g., batch, continuous).
04
Optimize the separation: Adjust the operating parameters of the chromatography system, such as flow rate, buffer composition, and gradient conditions, to optimize the separation of the bioformrapeutics. Monitor the separation using appropriate detection methods and adjust as needed.
05
Collect and analyze fractions: Collect the eluted fractions from the chromatography column and analyze them using suitable analytical techniques (e.g., UV spectroscopy, mass spectrometry). Evaluate the purity and yield of the bioformrapeutics to ensure successful purification.

Who needs continuous chromatography for bioformrapeutics:

01
Biopharmaceutical companies: Continuous chromatography is particularly valuable for large-scale production of bioformrapeutics, as it offers higher productivity, improved efficiency, and cost savings compared to traditional batch chromatography methods.
02
Research laboratories: Continuous chromatography can also be useful in research settings, allowing for rapid purification and characterization of bioformrapeutics samples. It enables researchers to obtain purified samples more quickly and efficiently, facilitating their studies and experiments.
03
Contract manufacturing organizations (CMOs): CMOs, which provide manufacturing services for biopharmaceutical companies, can benefit from continuous chromatography for bioformrapeutics purification. It allows them to streamline their operations and meet the high demands of their clients while maintaining quality and cost-effectiveness.
In summary, continuous chromatography for bioformrapeutics is essential for the purification and production of these therapeutic agents. It provides a more efficient and cost-effective method for obtaining pure bioformrapeutics samples, making it useful for biopharmaceutical companies, research laboratories, and contract manufacturing organizations.
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Continuous chromatography for bioformrapeutics is a method used in the purification process of biopharmaceuticals to enable the separation of different biomolecules based on their specific properties.
Biopharmaceutical companies and manufacturers who are involved in the production and purification of bioformrapeutics are required to file continuous chromatography reports.
Continuous chromatography reports for bioformrapeutics should be filled out with detailed information on the chromatography process, including the parameters used, the results obtained, and any deviations from expected outcomes.
The purpose of continuous chromatography for bioformrapeutics is to ensure the purity and quality of biopharmaceutical products by effectively separating different biomolecules and impurities.
The information to be reported on continuous chromatography for bioformrapeutics includes details on the chromatography process, equipment used, parameters set, results obtained, and any deviations or issues encountered.
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