Abstract: The present invention is directed to the development of continuous processing technology for the purification of biopharmaceuticals and biological products, such as monoclonal antibodies, protein therapeutics, and vaccines. Methods for continuous processing of a biological product in a feed stream toward formulation of a purified bulk product are described.

Abstract: The present invention is directed to the development of continuous processing technology for the purification of biopharmaceuticals and biological products, such as monoclonal antibodies, protein therapeutics, and vaccines. Methods for continuous processing of a biological product in a feed stream toward formulation of a purified bulk product are described.

Abstract: The present invention is directed to the development of continuous processing technology for the purification of biopharmaceuticals and biological products, such as monoclonal antibodies, protein therapeutics, and vaccines. Methods for continuous processing of a biological product in a feed stream toward formulation of a purified bulk product are described.

Abstract: Novel methods and devices are disclosed for automatically producing a simulated moving bed chromatography system and parameters from input of a fixed-bed liquid chromatography process directed at separating the same product. Tools and algorithms are provided which automatically convert fixed-bed process parameters into an executable simulated moving bed chromatography program. Familiar tabular input interfaces and a unique circular phase map of the simulated moving bed system that is generated according to input data makes the methods and apparatus of the invention extremely user-friendly and easy to use.

Abstract: The invention relates to a method and an apparatus for carrying out a treatment in the presence of centrifugal force. The treatment may be a physical or a chemical treatment. For this purpose the first and second phase are brought into contact with each other. The second phase comprises a phase soluble in the first phase and a third phase dispersed in the soluble phase. According to the invention at least one liquid phase is supplied continuously to a chamber for treatment (2) with a course of treatment while the third phase, which is a non-aggregating phase, is dispersed finely over the breadth of the course of treatment by the first phase.