Redipor-Group-cut-2-min

prepared media is used in environmental monitoring and testing applications

Healthcare, pharmaceutical and industrial organisations use reliable, quality assured prepared media every day

Maintaining cleanrooms and other aseptic areas to the most stringent regulations, plus validating sterility testing processes, requires quality assured prepared culture media.

The latest draft revision of EU GMP Annex 1 highlights an increasing need for organisations operating in pharmaceutical and medical device manufacture, food preparation and other industrial sectors to reduce the risk of contamination wherever possible.

Cherwell supplies an extensive range of prepared cultured media including poured media plates, bottled media, dipslides, broth bags, ampoules and more.

We offer many media formulation options and can even create bespoke media and accessories to match the specific requirements of your organisation and facility.

 

 

Let's discuss your requirements

Prepared media: how it's used

Environmental monitoring and testing procedures

Poured culture media

Used in cleanrooms, isolators, operating theatres, offices, factories and waste processing sites

Key to environmental monitoring, settle plates are used in active and passive air sampling, while contact plates are used to test surfaces. Dipslides are used to test for the presence of microoganisms in liquids.

Bottled media

Used in pharmaceutical, food and sterility testing processes

There are many different kinds of bottled media. They are typically used to test for various microbes across healthcare products, food, water treatment samples, environmental samples and more. They are particularly useful for the cultivation and isolation of microbes.

Tryptic Soy Broth & Fluid Thioglycollate Medium

Used to detect bacteria and fungi

In the pharmacopoeia sterility test, TSB is used to detect aerobic bacteria and funghi, and FTM to detect anaerobic bacteria. TSB is also used in universal operator transfer validation, to ensure aseptic standards are met during fluid transfer between different containers.

Some of our clients

Bespoke requirements? We can help

1_1
3_1
8_1
5_1
6_1
4_1

FREQUENTLY asked questions

About Prepared Media

Our environmental monitoring requirements have changed. Can you help us create new processes?

Yes. We have almost thirty years' experience with helping pharmaceutical and associated industries deliver environmental monitoring processes critical to the manufacture of heavily regulated products.

We supply every component you need to create environmental monitoring processes. We also offer bespoke formulations, accessories and even packaging solutions for organisations with very particular needs.

Get in touch today. Let's discuss your requirements.

Do I need to store my prepared media in the fridge?

The majority of our prepared media can be stored in ambient conditions, not exceeding 25ºC. There are only a small number of very specialist products that require different storage conditions.

We have never specified refrigeration as a storage condition for our general media as this causes excess condensation and can result in very wet agar, rendering it impossible to use.

What is the maximum exposure time for settle plates?

Settle plates are used to monitor the level of viable particles in the environment through a process of passive air sampling. A viable particle settles on agar plates at a rate dependent on its characteristics and the airflow in the environment.


EU GMP Guide Annex 1 has recommended that 90mm settle plates can be exposed in cleanroom environments for up to 4 hours. However, agar plates may dry out during long exposures where the rate of air exchange is high. So, it might be necessary to use deep filled settle plates, or replace the settle plate after a shorter time to ensure satisfactory growth promotion after exposure.

What is the difference between general purpose and selective growth media?

General purpose media have nutrients that support the growth of most non fastidious culturable microorganisms.

Selective growth media contain components that will inhibit the growth of some types of microorganisms, while supporting the growth of others.

General purpose media, such as Tryptone Soya Agar, are used to produce total counts. While selective media, such as XLD for Salmonella species, are used to test presence/absence of specific types of microorganism.

How much air should we sample?

Typical requirements suggest 1,000 litres per air sample in high risk areas, such as: grade A filling lines, grade B clean rooms, operating theatres etc. As the criticality of the area reduces, the sample size can be reduced. The aim is to achieve a representative sample; so where higher counts would be expected, a smaller sample produces a more realistic number of cfu to count.

Should I use contact plates or Petri dishes in my air sampler?

SAS samplers were originally designed for Contact plates, however, a Petri dish option has been available for a number of years. It is really a personal choice, although this should be decided at time of purchase, as the sampler will be specifically configured for the plate type chosen. There are advantages for each version and we would be happy to discuss your specific needs.

cherwell are environmental monitoring experts

Prepared media, equipment, accessories and services in one place

cherwell-icon-33

Getting it right from the start

Tell us about your business and we can help design the best EM solutions for you including prepared media, equipment and accessories

cherwell-icon-06

Quality assured products

Our products all come with quality assurance certification, manufactured in our ISO 9001 registered facility, delivered to order

cherwell-icon-39

Flexible service options

All formulations, consignment sizes and bespoke requirements considered. Our flexible service is tailored to your business

cherwell-IM-guide

get our latest environmental monitoring ebook

The Environmental Monitoring Processes and Validation Guide

Understand the key changes and challenges of the EU GMP Annex 1 draft revision.

What will it mean for your environmental monitoring processes?

Download Guide