spacer
home > pmps > winter 2002 > the scope of validation for cleanroom disinfectants
PUBLICATIONS
Pharmaceutical Manufacturing and Packing Sourcer

The Scope of Validation for Cleanroom Disinfectants

The validation of disinfectants for use in controlled environments can be both lengthy and expensive. This article examines the scope of disinfectant validation and how to ensure a smooth and successful outcome. As a disinfectant manufacturer we have a unique perspective on validation as not only do we have an in-depth knowledge of disinfectants but we also operate cleanrooms to the same cGMP standards as pharmaceutical manufacturers. It also allows us to gain a broad range of experience across the many life science fields including the pharmaceutical, biotechnology and medical device industries where similar issues arise repeatedly. The message is simple: consider all aspects of new agents right from the start. This will produce quick and meaningful validation results, which subsequently leads to early implementation of new disinfectants and prompt responses to audits.

Read full article from PDF >>

Rate this article You must be a member of the site to make a vote.  
Average rating:
0
     

There are no comments in regards to this article.

spacer
By Andrew Davidson, Commercial Director of Shield Medicare Ltd
Andrew Davidson is the Commercial Director of Shield Medicare Ltd. His qualifications include a BSc (Hons) in Biological Sciences and a CIM Diploma in Marketing. He has been with Shield Medicare for six years, having been recruited to develop the contamination control business. Before this he worked in the pharmaceutical industry for 15 years in both sales and marketing and product development roles.

spacer
Andrew Davidson
spacer
spacer
Print this page
Send to a friend
Privacy statement
News and Press Releases

AstroNova introduces its range of grass paper labels derived from grass for high quality organic products

Dietzenbach, 29 April 2019, AstroNova GmbH, European headquarters of AstroNova Inc. (RI, USA), responsible for Sales and Customer Service in Europe, the Middle East and Africa (EMEA), is extending its Product Identification range with new approved labelling for direct foodstuff contact.
More info >>

White Papers

Cleaning Validation: What do you need to consider to ensure a successful outcome?

RSSL

Cross contamination must be avoided in the Pharmaceutical industry at all costs and successful cleaning validation ensures that patients are not put at risk due to cross contamination. The process can be divided into a number of sections each of which must be fully understood and areas of concern addressed to ensure a successful outcome across the entire process. This spans both the manufacturing and subsequent analytical and microbological support. The data used to confirm a positive/successful cleaning validation is underpinned by the results of validated analytical methods. It is essential that these results are truly representative as patient safety is based upon the absence of equipment residues. So what are those areas of concern, what affects your ability to get a successful outcome and what do you need to consider when carrying out a Cleaning Validation exercise?
More info >>

 
Industry Events

Multimodal 2019

18-20 June 2019, NEC, Birmingham, UK

Now in its twelfth year, Multimodal is the UK and Irelandís premier freight transport, logistics and supply chain management event.  Shippers and cargo owners attend to improve their businesses; by finding ways of moving their products more efficiently and by meeting new suppliers. 
More info >>

 

 

©2000-2011 Samedan Ltd.
Add to favourites

Print this page

Send to a friend
Privacy statement