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    Aseptic manufacturing

    Aseptic manufacturing is a technique used to produce food or pharmaceutical products that don't require refrigeration. Following sterilization by exposure to heat, products are packaged into sterile containers. The entire packing procedure is also done under sterile conditions. Examples of foods commonly produced using aseptic manufacturing include tomato sauce, salad dressing, and fruit juices.

    What's Popular in Aseptic manufacturing

    Trending News

    • MAR 04, 2024
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      OCT 20, 2017
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    MAR 04, 2024
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    Webinars

    • NOV 17, 2021 | 11:00 AM
      ICH Q2 Validation of Analytical Procedures for Pharmaceutical Total Organic Carbon Analyzers
      ICH Q2 Validation of Analytical Procedures for Pharmaceutical...
      Date: November 17, 2021 Time: 11:00am (PDT), 2:00pm (EDT) The tripartite International Conference on Harmonisation (ICH) Q2 guide on validation of analytical procedures is not new, but it ca...
      Speaker: Tony Harrison
      Sponsored By: Beckman Coulter Life Sciences
      6
      JUL 28, 2021 | 10:00 AM
      GMP Cleanroom Routine Environmental Monitoring & 21CFR part 11 Data Integrity
      GMP Cleanroom Routine Environmental Monitoring & 21CFR part 11...
      Date: July 28, 2021 Time: 10:00am (PDT), 1:00pm (EDT) Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points...
      Speaker: Tony Harrison
      Sponsored By: Beckman Coulter Life Sciences
      11
      MAY 27, 2021 | 10:00 AM
      Changes to USP <1788> Subvisible Particulate Matter
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      DATE: May 27, 2021 TIME: 11:00am PDT A revised version of the USP chapter on Total Organic Carbon (TOC) USP<643> was published recently and will become official on 1 st May 2021. This...
      Speaker: Tony Harrison
      Sponsored By: Beckman Coulter Life Sciences
      5
      APR 28, 2021 | 11:00 AM
      Changes to USP <643> Total Organic Carbon for Pharmaceutical Grade Waters
      Changes to USP <643> Total Organic Carbon for Pharmaceutical Grade...
      DATE: April 28, 2021 TIME: 11:00am PDT A revised version of the USP chapter on Total Organic Carbon (TOC) USP<643> was published recently and will become official on 1 st May 2021. Thi...
      Speaker: Tony Harrison
      Sponsored By: Beckman Coulter Life Sciences
      5
      DEC 14, 2020 | 10:00 AM
      Testing Vaccines final dose form to USP<787> Subvisible Particulate Matter
      Testing Vaccines final dose form to USP<787> Subvisible Particulate...
      DATE: December 14, 2020 TIME: 10:00am PST USP chapter <787>, Subvisible Particulate Matter in Therapeutic Protein Injections, became official August 1, 2014 and provides specific guida...
      Speaker: Tony Harrison
      Sponsored By: Beckman Coulter Life Sciences
      7
    NOV 17, 2021 | 11:00 AM
    ICH Q2 Validation of Analytical Procedures for Pharmaceutical Total Organic Carbon Analyzers
    ICH Q2 Validation of Analytical Procedures for Pharmaceutical...
    Date: November 17, 2021 Time: 11:00am (PDT), 2:00pm (EDT) The tripartite International Conference on Harmonisation (ICH) Q2 guide on validation of analytical procedures is not new, but it ca...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
    6
    JUL 28, 2021 | 10:00 AM
    GMP Cleanroom Routine Environmental Monitoring & 21CFR part 11 Data Integrity
    GMP Cleanroom Routine Environmental Monitoring & 21CFR part 11...
    Date: July 28, 2021 Time: 10:00am (PDT), 1:00pm (EDT) Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
    11
     
     
    MAY 27, 2021 | 10:00 AM
    Changes to USP <1788> Subvisible Particulate Matter
    Changes to USP <1788> Subvisible Particulate Matter
    DATE: May 27, 2021 TIME: 11:00am PDT A revised version of the USP chapter on Total Organic Carbon (TOC) USP<643> was published recently and will become official on 1 st May 2021. This...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
    5
    APR 28, 2021 | 11:00 AM
    Changes to USP <643> Total Organic Carbon for Pharmaceutical Grade Waters
    Changes to USP <643> Total Organic Carbon for Pharmaceutical Grade...
    DATE: April 28, 2021 TIME: 11:00am PDT A revised version of the USP chapter on Total Organic Carbon (TOC) USP<643> was published recently and will become official on 1 st May 2021. Thi...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
    5
    DEC 14, 2020 | 10:00 AM
    Testing Vaccines final dose form to USP<787> Subvisible Particulate Matter
    Testing Vaccines final dose form to USP<787> Subvisible Particulate...
    DATE: December 14, 2020 TIME: 10:00am PST USP chapter <787>, Subvisible Particulate Matter in Therapeutic Protein Injections, became official August 1, 2014 and provides specific guida...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
    7
    OCT 23, 2020 | 7:00 AM
    Quality Control Electronic Records for 21CFR part 11 Data Integrity
    Quality Control Electronic Records for 21CFR part 11 Data Integrity
    DATE: October 23, 2020 TIME: 07:00am PDT, 10:00am EDT The FDA’s 21CFR part 11 guidance on the use of electronic records for data retention or submission is clear. With manually implemen...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
    4
    SEP 29, 2020 | 8:00 AM
    Microbial Quality Control in Manufacturing of Medicinal Products
    Microbial Quality Control in Manufacturing of Medicinal Products
    DATE: September 29, 2020 TIME: 8:00 am PDT There is a steady increase in FDA 483s related to microbiology. Though most are for sterile products, non-sterile and terminally sterilized product...
    Speaker: Ziva Abraham
    Sponsored By: Sartorius
    19 5
    SEP 09, 2020 | 10:00 AM
    Classification and Routine Environmental Monitoring for GMP Cleanrooms
    Classification and Routine Environmental Monitoring for GMP Cleanrooms
    DATE: September 09, 2020 TIME: 10:00am PDT, 1:00pm EDT The various GMP guidelines and International ISO standards around GMP cleanrooms are complex and often appear to give conflicting advic...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
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    AUG 12, 2020 | 10:00 AM
    GMP Cleanroom Routine Environmental Monitoring & 21CFR part 11 Data Integrity
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    DATE: August 12, 2020 TIME: 10:00am PT Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points per month, man...
    Speaker: Tony Harrison
    Sponsored By: Beckman Coulter Life Sciences
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    SEP 05, 2017  | 8:00 AM PDT
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