By Andy Whittard

What Training Should your Cleanroom Manufacturing Staff Undergo?

By definition, the cleanroom environment is no place for a laissez-faire attitude. With a number of regulatory protocols applying to pharmaceutical manufacture, the chance of falling short is a very realistic risk – and it takes diligence and scrupulous protocol to maintain regulatory standards.

Read More
GPT guide cta-min-1

Growth Promotion Testing: A Guide to Good Practices

Get an in-depth understanding of key considerations and best practices when undertaking growth promotion testing (GPT).
Download Guide

By Andrew Ramage

The Weakest Link in the Cleanroom Environment? Humans

By Andrew Ramage

Why Cleanroom Operators Choose Cherwell as Supplier

By Andrew Ramage

Cleanroom Operators - Recommended Research Papers: Oct 2016 - Apr 2017

By Andrew Ramage

PHSS June 2017 Conference Review

By Andrew Ramage

Making Pharmaceuticals 2017

By Wan Li Low

Desiccation of Agar Plates

We promise that we won't SPAM you.

What's next

Recent news

Navigating the Glass vs Plastic Dilemma in Pharmaceutical Manufacturing

Navigating the Glass vs Plastic Dilemma in Pharmaceutical Manufacturing

12 December 2024
Pharmig 2024: Cherwell attends dynamic, inspiring, moving event

Pharmig 2024: Cherwell attends dynamic, inspiring, moving event

09 December 2024

Subscribe

Receive the latest articles as they are published.

Contact us

Registered Office


7 & 8 Launton Business Centre,
Murdock Road,
Bicester,
OX26 4XB

Phone
Tel: +44 (0) 1869 355 500
Fax: +44 (0) 1869 355 545

Email
sales@cherwell-labs.co.uk

 
Cherwell_Logo+claim2_RGBx200
Cherwell Laboratories ©2018
Reg. in England No: 01159518
VAT Reg. No: GB 121 6903 94

Copyright © 2022 Cherwell Laboratories. All rights reserved. Privacy Policy & Disclaimer