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Cleaning Validation – Are YouMeeting Regulatory Requirements?
Cleaning Validation, a GMP requirement, is key to the manufacturing process. Effective cleaning is essential to protect patient safety, and cleaning processes must be proven to remove active pharmaceutical ingredient residues, cleaning materials, and any microbial contamination that could put patients at risk due to cross-contamination. Cleaning validation is a critical aspect of quality control, and necessary for ensuring your product is fit for release.
Reading Scientific Services Ltd
The Reading Science Centre, Whiteknights Campus, Pepper Lane, Reading, Berkshire RG6 6LA
Tel: +44 (0)118 918 4076 Email: [email protected] Web: www.rssl.com
Our cleaning validation services will:
• Test and challenge your cleaning regime
• Demonstrate compliance with GMP
requirements
• Allow you to manufacture with confidence
• Facilitate process improvements and
productivity gains
• Equip your staff to implement better
hygiene
RSSL’s Cleaning Validation ServicesRSSL is an established expert in this field and we have a coordinated approach to cleaning validation
with unique manufacturing consultancy, chemical analysis, microbiological analysis and training
services. We can support you with cleaning validation, both for due diligence and troubleshooting
issues, ensuring you satisfy regulatory requirements.
Our experts can advise and support you with inspections of manufacturing sites. ‘Walking the Plant’
can help get to the root of where residues are difficult to remove and therefore pose considerable
threat to batch to batch contamination.
Contact us to find out more about our expertise and how we can support you:Tel: +44 (0)118 918 4076 Email: [email protected] Web: www.rssl.com
Reading Scientific Services Ltd
The Reading Science Centre, Whiteknights Campus, Pepper Lane, Reading, Berkshire RG6 6LA
RSSL can support you with:
• Validation of cleaning procedures
• Microbiological and chemical analyses of
swabs and rinses
• Expert interpretation, support and advice
• Development of and validation of
analytical methods
• Testing the efficacy of your disinfectants
• Process improvement
• Troubleshooting
• Cleaning validation training
• Consultancy
