Our Offering
Technical Services
Your partners for continuous improvement
Expert implementation of regime change in cleanrooms
Request the ebookThe need for process change
In such a highly regulated environment, change is not undertaken lightly. As a result, a lack of internal resources can often obstruct the implementation of change.
Continuous improvement is a drive for better practices across the pharmaceutical industry, lead by an FDA initiative. There are many factors driving continuous improvement in your cleaning, disinfection and bio-decontamination practices including:
Quality & Compliance
Operational Efficiency
Global Harmonisation
Sustainability
Safety
Cost Savings
Our team of Global Technical Consultants can help make positive changes to your processes, driving continuous improvement that helps meet quality and regulatory requirements and business objectives.
Highly experienced in key topics including regulatory compliance, residue management and disinfectant efficacy validation, a partnership with Ecolab provides expert guidance and implementation support to ease the burden of change in your cleanroom.
Ecolab’s Change Management Program
for cleaning, disinfection & bio-decontamination
Ecolab’s Change Management program provides you with a customised plan that meets your specific needs, supporting you through an end-to-end process, comprising one or more of the following elements.
1. Risk Assessment
Identifying the need for change
- On-site/virtual assessment of contamination risks against industry regulations and best practice
- Detailed reporting of risks and mitigations supporting the contamination control strategy
2. Supplier Assurance
Assess suitability of your supplier:
- Vendor qualification support
- Documentation to support your change control process
3. Product Selection
Selecting the products and equipment to implement:
- Support with automated and manual product selection specific to your requirements
- Bespoke regime designed to mitigate contamination risks
4. Validation
Prove the selected agents and regime control contamination within the facility:
- Validation project management
- Disinfectant efficacy testing
- In-situ validation study design
5. Implementation
Generating the resources required for the execution of your operation:
- Updating / creating standard operational documents
- Training theory and practice
- Ongoing technical support service
NEW eBook: Continuous Improvement
Request our new eBook to find out more about how our team of experts can help implement positive changes to the cleaning, disinfection and bio-decontamination measures in your cleanroom.
REQUEST THE EBOOK
Leverage Ecolab’s expertise to ease the acceptance, approval and implementation of change so that you can focus on the core of your pharmaceutical business.
Ecolab’s Change Management programme
Speed up the implementation of change
Reduce associated costs and resources
Help with compliance and audit readiness