A method of controlling additive delivery during a bioreaction in a bioreactor comprises running a bioreaction in a bioreactor including adding additive into the bioreactor during spaced-apart feed events, where contents of the bioreactor equilibrate during a stabilisation period after a feed event; making in situ measurements of a bulk physical property of the bioreactor contents during the bioreaction to obtain process trend data; calculating a derivative of process trend data obtained over a measurement period beginning after a stabilisation period, the derivative being a metabolic rate index (MRI); and using the MRI to determine a time for starting a next feed event. A controller for a bioreactor and a bioreactor system are configured to operate according to the method.

A method of controlling additive delivery during a bioreaction in a bioreactor comprises running a bioreaction in a bioreactor including adding additive into the bioreactor during spaced-apart feed events, where contents of the bioreactor equilibrate during a stabilisation period after a feed event; making in situ measurements of a bulk physical property of the bioreactor contents during the bioreaction to obtain process trend data; calculating a derivative of process trend data obtained over a measurement period beginning after a stabilisation period, the derivative being a metabolic rate index (MRI); and using the MRI to determine a time for starting a next feed event. A controller for a bioreactor and a bioreactor system are configured to operate according to the method.

An exemplary embodiment of an apparatus for detecting microbiological activity in an industrial process may include a plurality of satellite units, a processing unit, and a main analysis unit. Each satellite unit may be configured to sample a liquid from the industrial process at a plurality of respective locations, periodically analyse a sample, carry out an impedance analysis to count and measure the size of particles passing through an orifice, and generate sample results data corresponding to the number and size of particles in each sample. The processing unit may be configured to compare the sample results data to a predetermined criterion and to generate an alert signal if the particle data is outside of the predetermined criterion. The main analysis unit may be configured to carry out a combined impedance and electromagnetic emission analysis of a sample of liquid from the industrial process following generation of the alert signal.

An exemplary embodiment of an apparatus for detecting microbiological activity in an industrial process may include a plurality of satellite units, a processing unit, and a main analysis unit. Each satellite unit may be configured to sample a liquid from the industrial process at a plurality of respective locations, periodically analyse a sample, carry out an impedance analysis to count and measure the size of particles passing through an orifice, and generate sample results data corresponding to the number and size of particles in each sample. The processing unit may be configured to compare the sample results data to a predetermined criterion and to generate an alert signal if the particle data is outside of the predetermined criterion. The main analysis unit may be configured to carry out a combined impedance and electromagnetic emission analysis of a sample of liquid from the industrial process following generation of the alert signal.

A cell recovery apparatus includes an observation apparatus for observing the inside of a medium in a container via an insertion section to be inserted into the medium, and a recovery apparatus that is positioned relative to a predetermined region to be observed by the observation apparatus and recovers a cell in the medium from the container.

A cell recovery apparatus includes an observation apparatus for observing the inside of a medium in a container via an insertion section to be inserted into the medium, and a recovery apparatus that is positioned relative to a predetermined region to be observed by the observation apparatus and recovers a cell in the medium from the container.

Systems and methods are provided for sample processing. A device may be provided, capable of receiving the sample, and performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing multiple assays. The device may comprise one or more modules that may be capable of performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing the steps using a small volume of sample.

Systems and methods are provided for sample processing. A device may be provided, capable of receiving the sample, and performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing multiple assays. The device may comprise one or more modules that may be capable of performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing the steps using a small volume of sample.

An extra-capillary fluid cycling unit for maintaining and cycling fluid volumes in a cell culture chamber includes a housing and a first flexible reservoir extra-capillary fluid reservoir disposed in the housing. The extra-capillary fluid reservoir is in fluid communication with a cell culture chamber. A second flexible reservoir is also located in the housing, the second flexible reservoir being in fluid communication with a pressure source. A sensor plate is movably disposed in the housing between the extra-capillary reservoir and the second reservoir, wherein the second reservoir is pressurized to move the sensor plate in relation to the extra-capillary reservoir to cause fluid cycling and maintain fluid volumes in the cell growth chamber.

An extra-capillary fluid cycling unit for maintaining and cycling fluid volumes in a cell culture chamber includes a housing and a first flexible reservoir extra-capillary fluid reservoir disposed in the housing. The extra-capillary fluid reservoir is in fluid communication with a cell culture chamber. A second flexible reservoir is also located in the housing, the second flexible reservoir being in fluid communication with a pressure source. A sensor plate is movably disposed in the housing between the extra-capillary reservoir and the second reservoir, wherein the second reservoir is pressurized to move the sensor plate in relation to the extra-capillary reservoir to cause fluid cycling and maintain fluid volumes in the cell growth chamber.