Examples of using Aseptic processing in English and their translations into German
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The investment costs are lower than those for aseptic processing.
For products requiring aseptic processing, various rinsing machines are available.
CFM(28.3 L/min) flow rate, up to four channels ofparticle data including 0.5μm per US FDA Aseptic Processing Guidelines.
Description: Validation of aseptic processing should include a simulation test using a nutrient medium, known as the media fill or media simulation test. The selec….
Process validation and/or evaluation studies for aseptic processing and sterilization should be included.
The Concentrating Pipette can be employed in numerous areas of quality control, environmental control and aseptic processing like.
For the validation of aseptic processing of parenteral products that cannot be terminally sterilized, simulation process trials should be conducted.
Ampack is the technology leader in the segment of near-sterile and aseptic processing of pre-formed cups and bottles.
Technologies such as lyophili sation, aseptic processing of injection solutions, sterile crystallisation, sterile filling of powders into injection bottles and nanotechnological procedures are used here.
Existing portfolio expanded to include the area of low-germ and aseptic processing of pre-formed cups and bottles.
Description, documentation, and results of the validation and/or evaluation studies should be provided for critical steps or critical assays usedin the manufacturing process e.g. validation of the sterilization process or aseptic processing or filling.
Ampack Ammann is a technological leader in the area of low-germ and aseptic processing of pre-formed cups and bottles.
Other services We use our extensive experience in the areas of Good Manufacturing Practice,advanced therapy medicinal products, aseptic processing and cellular analysis, to stand by your side and offer not only our expert opinion, advice and training but also logistical support during the process establishment and validation as well as clean room capacity for your projects. Print page.
Complete the form on this page to receive a free copy of theMicrobial Control and Monitoring in Aseptic Processing Cleanrooms application note.
Coupon materials not representative of floors, walls, and work surfaces in the aseptic processing area including worn or damaged surfaces.
TSI's cleanroom monitoring solutions for life science applications help youcomply with regulations such as the FDA Guidance on Aseptic Processing 2004 and EU GMP Annex 1:2009.
A RABS or isolator-based robotic system, implemented according to ANSI/RIA R15.06 standards,will provide a robot cell that meets requirements for Advanced Aseptic Processing in the pharmaceutical industry.
Environmental Monitoring(EM), particularly in Pharmaceutical manufacturing facilities where therisk of microbial contamination is controlled through aseptic processing, comprises both physical and microbiological test methods.