Abstract:
Sample contamination is suppressed by strengthening the air barrier of a work opening portion. A safety cabinet includes: a work room; a front surface door covering a part of a front opening portion of the work room; and a work opening portion on a lower side of the front surface door allowing a worker to work with his or her hand in. An intake port suctions air in the work room and outside air through the work opening portion on a front surface side of a workbench in a lower portion of the work room. A straightening plate drawing an air flow and a linear light source are provided on the work room side of the front surface door and above a front portion of the work room.
Abstract:
A weighing fume cupboard (1) for weighing pharmaceutically active or toxic substances in a laboratory, comprising a housing (10) which defines a working space (19), wherein a front side of the housing (10) has a working opening (11) which is open at all times during intended use of the weighing fume cupboard (1), a working plate (20) which delimits the working space (19) at the bottom side, an armrest (40) in the region of the working opening (11), and a support (30) which bears the weight of the housing (10), of the working plate (20) and of the armrest (40), wherein, during intended use of the weighing fume cupboard, the working plate (20) is decoupled in terms of shocks and vibrations from the housing (10), from the armrest (40) and from the support (30).
Abstract:
Biosafety units, methods of making and sealing the same are disclosed herein. The present invention includes a unitary structure able to be validated for pharmaceutical manufacturing comprising: at least one controlled air, sealable, sterilizable cleanroom; a mechanical system room adjacent to and separate from the cleanroom comprising: one or more air handling units that provide conditioned air to the cleanroom; and one or more power busses that provide power to electrical outlets in the cleanroom from two sources, wherein the at least two power supplies are connectable to one or more external electrical power sources; an integrated fire suppression system integral to the cleanroom; and one or more corridor connectors, wherein a corridor can be attached at the corridor connector.
Abstract:
Biosafety units, methods of making, and sealing the same are disclosed herein. The units comprise at least one controlled air, sealable, sterilizable cleanroom; and a mechanical system room adjacent to the cleanroom comprising: at least two air handling units in a support room adjacent the cleanroom that provide redundant air to the cleanroom with at least Class 100,000 air purity, the air handling units connected to a one or more supply ducts to the cleanroom, and an exhaust duct in communication with the cleanroom and the air handling unit exhaust, wherein a pressure gradient is formed between the cleanroom and the exterior of the structure; and at least two power supplies that provide redundant power to electrical outlets in the cleanroom, wherein the at least two power supplies are connectable to one or more external power sources and the structure is pre-validatable or validated for pharmaceutical manufacturing.
Abstract:
A work area is disposed in a conveyance path for cells and has an inlet and an outlet, with a downflow air curtain provided at least at the inlet and the outlet. A conveyor repeatedly performs an operation that moves a placement surface having a culture vessel thereon from the inlet side into the area, moves the placement surface from the outlet side to the outside of the area, and, subsequently, moves back the placement surface to the inlet side. The cleaning device cleans the placement surface during the period from when the conveyor in the work area moves the placement surface to the outside of the area until the conveyor moves back the placement surface to the inlet side of the area.
Abstract:
It is constituted such that a sterile work can be applied by a worker 29 to cells or the like through a glove 28 provided in an isolator 15. A headset 31 for work outputting a work procedure of the sterile work in voice is prepared for the worker, and an input device 39 for check is prepared for a checker 36. A management device 12 outputs the work procedure of the sterile work this time in voice to the headset for work. When the fact that the worker has normally performed the sterile work this time is checked by the checker, and when the fact is input from the input device for check to the management device, the management device performs the subsequent work procedure.Since the sterile work by the worker 29 can be monitored by the checker 36, a wrong work can be prevented from being performed.
Abstract:
A biosafety cabinet includes one or more air filters below the work surface and a system for holding, sealing, replacing and disposing the air filters through the work access opening of the biosafety cabinet. The air filters under the work surface of the biosafety cabinet capture particulates entering the cabinet from the exterior environment and the particulates within the cabinet's work chamber. Instead of a mechanical clamp, the perimeter of the air filters are sealed using a gasket and a tape, eliminating the accumulation of the contaminants around mechanical clamps. The air filters may be accessed through the work access opening of the biosafety cabinet, packaged for disposal and removed from the biosafety cabinet without being exposed to the exterior environment. A filter cover with an adhesive surface is used to cover and lift the used, contaminated air filter within the biosafety cabinet.
Abstract:
A filter unit which has a simple structure and can ensure high-level safety in response to risk during operation of an apparatus such as an isolator device is provided. One type of filter unit includes a rectangular cylindrical body having a first wall portion provided with an air inlet portion and a second wall portion formed so as to cross the first wall portion and provided with an air discharge port portion, a filter member provided in the cylindrical body for filtering introduced air, an annular seal member surrounding an outer periphery portion of the air inlet portion, and a detachable lid body closing the air inlet portion in an airtight manner. The filter unit is connected to a work chamber such that the air inlet portion is attached so as to oppose an air outlet of the work chamber and so that the seal member abuts an outer wall portion of the work chamber in an airtight manner.
Abstract:
In a system and method of controlling particulate count in a clean room having a number of compartments/zones in series, in response to a first level of energy consumption by speed adjustable fans supplying a first volume of air per unit of time to the clean room, differential air pressures are established in the clean room compartment/zone-by-compartment/zone in series from a first compartment/zone which has a requirement for the highest air pressure to a last compartment/zone which has a requirement for the lowest air pressure. In response to a second level of energy consumption by the speed adjustable fans supplying a second volume of air per unit of time to the clean room, the same differential air pressures are substantially maintained in the clean room.
Abstract:
An isolation booth for creating a locally isolated space, includes: a top portion; a bottom portion; a curtain rail that is provided on at least one of the top portion and the bottom portion; and a curtain member that is in an endless belt shape and has a ring shape when viewed from above, is supported by the curtain rail in a manner so as to be able to be moved along the curtain rail, and is provided so as to create the space between the top portion and the bottom portion, the curtain member including a glove member that bulges out toward an inside of the space.