A brief history of the impaction sampler

By Andy Whittard

How modern microbial air samplers can be traced back to the 19th century

Microbial air sampling within the pharmaceutical and associated industries has become a vitally important tool within GMP manufacturing. The instruments available today are varied in both size and style, but most employ a very old technique – that is impaction, into or onto, a collection medium. Which got me thinking, where do they originate from?

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Continuous environmental monitoring is key in Annex 1

By Andy Whittard

As the European Pharma industry becomes more familiar with the GMP Annex 1 draft revision, it is clear that continuous environmental monitoring (EM) is going to become increasingly important.

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Cherwell supports conference addressing novel challenges in aseptic manufacturing of advanced medicinal therapeutics

By Gill Power

New biological and ATMP therapies require alternative GMP framework

 Bicester, UK, 24th August 2018: Cherwell Laboratories, supplier of environmental monitoring and process validation products, has confirmed its continued support for the Pharmaceutical & Healthcare Sciences Society (PHSS) - UCL Q3P Annual Conference 2018. This year’s event will address the key challenges in manufacturing and aseptic processing in the new area of Biological and Advanced Therapy Medicinal products (ATMPs),...

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Environmental Monitoring: Implications of GMP Annex 1 for large pharma

By Andrew Ramage

The draft revision of the EU GMP Annex 1 has been received with mixed feelings. The European Medicines Agency (EMA) is currently working its away through the 6000+ comments that have come about since the release of this revision.

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Should hospital pharmacies review their environmental monitoring?

By Andrew Barrow

The revised EU GMP Annex 1 guidelines for manufacture of sterile medicinal products may still be some way off publication, but the latest draft revision offers highly relevant information that can be used to improve compliance and reduce risks.

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Cherwell Publishes Guide on Environmental Monitoring Processes and Validation

By Gill Power

 

Supporting EM programs in preparation for proposed EU GMP Annex 1 changes

 

Bicester, UK, 18th July 2018: Cherwell Laboratories, specialist supplier of products for environmental monitoring and process validation, has drawn on its in-depth pharmaceutical and related industry knowledge to publish an eBook titled, “The Environmental Monitoring Processes and Validation Guide.” 

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June 2018 visit with Redipor distributor - Sterbios

By Andrew Ramage

 

One of my many functions at Cherwell Laboratories is to be the first point of contact for all distributor enquiries. As mentioned in previous press releases we have enjoyed a significant increase in sales of Redipor® prepared media over the last few years to mainland Europe and South Korea. This is due in no small part to our distributors working very hard to establish the Redipor® brand in their territories and the high quality of the media sold. My job is to offer technical advice on...

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Environmental monitoring: How to maintain a cleanroom

By Andy Whittard

Your environmental monitoring (EM) program must demonstrate control over both viable and non-viable particles found in critical areas of your operation. The procedures and protocols you have in place must ensure asepticism throughout your operation.

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PHSS Annual Challenges in Sterile Product Manufacturing Meeting 2018

By Andrew Ramage

It is always a pleasure to attend the PHSS steriles meeting as there are always many fascinating topics being presented and discussed. This year had an excellent selection of talks about the latest trends and discussion points in the manufacture of sterile drugs. Sales Manager, Andrew Barrow and I attended on behalf of Cherwell Laboratories. The event was held on the 7th June, at The Mere Hotel & Spa in Knutsford for the second consecutive year.

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Cherwell enhances quality management system

By Gill Power

Cleanroom microbiology solutions provider completes transition to ISO9001:2015

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