Cherwell to offer practical advice and solutions on environmental monitoring and process validation
Bicester, UK, 25th August 2017: Cherwell Laboratories have confirmed their continued support for the Pharmaceutical & Healthcare Sciences Society (PHSS) - UCL Q3P Annual Conference 2017. A comprehensive range of specialist environmental monitoring and process validation products available from Cherwell will be on display on the company’s stand, with Cherwell staff available to demonstrate them and offer expert advice.
The annual conference, taking place on the 8th September 2017 at University College London (UCL) School of Pharmacy, is free-to-attend for PHSS members. The event will focus on “Challenges in Biological and Advanced Medicinal Therapeutic Product Manufacturing following GMP”. The agenda includes a PHSS guidance update on Environmental Control and Process Monitoring case study guidance initiative together with Clarity in GMP on challenging topics by James Drinkwater, Leader of PHSS Bio-contamination Special Interest and Focus groups.
Over its 45 years’ of experience, Cherwell has built a reputation within the pharmaceutical and healthcare sciences industry as a provider of high-quality products to meet the specific requirements of environmental monitoring and process validation. The Cherwell range includes Redipor® prepared media; a selection of petri dishes, settle plates, bottled media, broth bags, vials and ampoules and SAS microbial air samplers.
Members of the Cherwell team will be on hand at the event to offer delegates advice and discuss customer-specific requirements. Andrew Ramage, Cherwell’s Microbiology Product Specialist, who will be attending the event, commented, “This year should provide a fascinating insight into the challenges faced by manufacturers of biologicals and advanced medicinal products. Monitoring and maintaining a high quality cleanroom environment is central to that success. We look forward to discussing the individual challenges delegates face and advising them on the most suitable solutions we can provide for their specific requirements”.
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?