Technical Services

Your partners for continuous improvement

Expert implementation of regime change in cleanrooms

Request the ebook

The 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.

Watch now: The Needs and Pains 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



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

Watch now: Change Management Programme Overview

Watch now: End-to-end Change Management

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.


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

Contact Us

With unparalleled expertise and cutting-edge technology, we partner with customers to deliver world-class results and optimized operations.

Contact us to learn how we can help you.


1 Ecolab Place
St. Paul, MN 55102


Richtistr. 7
8304 Wallisellen
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