Cherwell highlights products for environmental monitoring and process validation
By Gill Power
Cherwell keeps up to date with Hospital Pharmacy QA requirements
Bicester, UK, September 2013: Cherwell Laboratories, experts in environmental monitoring and process validation will be demonstrating their comprehensive product range at the NHS Pharmaceutical QA Symposium for Technical Services on 24th & 25th September 2013.
The annual QA Symposium, to be held at Crowne Plaza, Chester is aimed at pharmacy professionals working in pharmaceutical production and quality assurance environments within the NHS or commercial sector. The event has been structured to encourage delegates to create their own experience around their individual needs and interests with a variety of presentations and workshops plus an exhibition area featuring pharmaceutical companies and equipment suppliers.
It is an excellent opportunity for both delegates and suppliers to keep up to date with the QA requirements for hospital pharmacies and to improve performance and delivery of services.
Cherwell Laboratories will be displaying their range of specialist products for environmental monitoring and process validation whilst offering practical advice and support to delegates. The Cherwell product range on display will include a selection of Redipor Prepared Media products; such as petri dishes, settle plates, bottled media, broth bags, vials and ampoules. A range of biological indicators for validation of sterilisation processes and SAS microbial air samplers for environmental monitoring will also be available.
“We are very happy to have supported this annual meeting for several years” commented Andrew Barrow, Sales Manager, Cherwell Laboratories. He added “Cherwell works with their customers to provide the most appropriate solution for their individual requirements, and will be available throughout the event to discuss any specific requirements”.
For more information about our environmental monitoring and process validation product range please contact us.
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?