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9th March 2021  Content supplied by: various sources as indicated

Sterility Testing - A rapidmicrobiology Special Focus


Sterility assurance is critical in the manufacture of many drugs and other medicinal products and is closely regulated worldwide. Products carrying a claim of sterility typically require some form of sterility test to be carried out before release in order to verify that claim.

In this rapidmicrobiology special focus you will discover the latest products in sterility testing, aswell as podcasts covering upcoming changes to Annex I and environmental monitoring. 

Straightforward Sterility Testing of your Viscous Samples with RTU Sterile IPM

Straightforward Sterility Testing of your Viscous Samples with RTU Sterile IPM

As the only supplier worldwide, we offer ready-to-use, sterile IPM validated for sterility testing of viscous products, such as creams and ointments, without time-consuming preparation.
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Jump Start Your RMM Validation for Sterility Testing

Jump Start Your RMM Validation for Sterility Testing

Reduce time from installation to routine use of Celsis® rapid sterility platform with Charles River's support packages, easily demonstrate validation parameters described by USP <1223>, Ph. Eur. 5.1.6, and PDA TR 33.
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Top 10 Requested Strains for Environmental Isolates and Objectionable Organisms

Top 10 Requested Strains for Environmental Isolates and Objectionable Organisms

In this feature, Microbiologics list & characterize the top 10 non-compendial objectionable organisms that are requested through their Custom Solutions program for environmental isolates and objectionable organisms.
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Growth Promotion Testing: A Guide to Good Practices

Growth Promotion Testing: A Guide to Good Practices

Cherwell Laboratories have a new ebook titled: "Growth Promotion Testing: A Guide to Good Practices". It is intended for anyone involved in growth promotion testing of microbiological media, particularly focusing on pharmaceutical and sterile medical device industry applications.
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Story of the Steritest™ Invention: How Millipore Made the Sterility Test Reliable in the 1970s

Story of the Steritest™ Invention: How Millipore Made the Sterility Test Reliable in the 1970s

Want to know how the Steritest™ system has been invented? Read the fabulous story of its invention to discover why and when it has been invented, and what were the challenges at this time.
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Cleanroom Microbiology Supplier, Cherwell Laboratories, Celebrates 50-year Anniversary

Cleanroom Microbiology Supplier, Cherwell Laboratories, Celebrates 50-year Anniversary

Leading UK-based manufacturer of prepared media and supplier of microbial monitoring equipment Cherwell Laboratories is 50 years old.  They plan to mark the occasion with various, events, competitions, and activities to mark the occasion. Find out how you can join in their fun celebrations.
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Special Focus on Using Rapid Microbiological Methods to Streamline Workflow in Vaccine Production

Special Focus on Using Rapid Microbiological Methods to Streamline Workflow in Vaccine Production

In this rapidmicrobiology special focus, you can browse through a range of rapid microbial methods that can help streamline production processes in vaccine development and production.
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Continuous Environmental Monitoring in New Annex I - a rapidmicrobiology podcast

Continuous Environmental Monitoring in New Annex I - a rapidmicrobiology podcast

In this episode, Andy Whittard (MD at Cherwell Laboratories) and Gethin Jones (MD at Pinpoint Scientific) lend their expertise to environmental monitoring in pharmaceutical manufacturing with a particular focus on changes to continuous monitoring in the proposed Annex I. 
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GMP Annex 1: Changes in Microbial Monitoring - a rapidmicrobiology podcast

GMP Annex 1: Changes in Microbial Monitoring - a rapidmicrobiology podcast

In this episode, Anne Klees and Adele Gisselmann (Global Product Managers with Merck KGaA Darmstadt, Germany) unravel the New GMP Annex I (Draft 2020) and explain what effect its changes and new sections will have on environmental microbial monitoring.
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How to Validate and Implement Your Rapid Microbiological Method - Interview With Dr. Michael Miller

How to Validate and Implement Your Rapid Microbiological Method - Interview With Dr. Michael Miller

Dr. Michael J. Miller, one of the leading global experts on rapid microbiology method validation and implementation, talks to rapidmicrobiology.com about the current status of rapid methods within the pharmaceutical and biopharmaceutical industries and how ATMPs is accelerating adoption.
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Date Published: 9th March 2021