Biotech and Pharma Consultancy
Electronic Qualification Services Ltd.
Modular GxP Validation & Compliance Specialists
“With more than 100,000 of our Validation Templates in use worldwide, there’s a strong chance your organization is already benefiting from our trusted and proven validation methodology.”
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Why Electronic Qualification Services Limited?
Since 1992, we have successfully delivered validation projects across active pharmaceutical ingredients (API), pharmaceuticals, biopharmaceuticals, and medical devices. Our collaborations with clients and regulatory authorities in the UK, Europe, the US, China, India, Taiwan, Hong Kong, Australia, and beyond have equipped us with a deep understanding of the cultural and regulatory complexities of the global compliance landscape.
With extensive experience spanning both greenfield and established sites, we have partnered with multinational corporations as well as start-ups. Our distinctive advantage lies in the diverse expertise of our team, which includes GxP manufacturing, engineering design, and contract validation services—providing us with a unique perspective on the full spectrum of industry challenges.
More than two decades ago, we recognized that traditional one-off validation and compliance projects often lacked both cost and time efficiency. In response, we began to develop products and services aimed at providing more sustainable, life-cycle-oriented continuous improvement solutions.
In particular, we have focused on addressing the validation and compliance challenges of two key sectors within the life sciences industry:
For GxP Drug Manufacturers we have developed continuous improvement models that:
- Can be implemented in a patchwork-like manner across the business, with different components prioritized and integrated gradually
- Can be rapidly overlayed over legacy validation packages to leverage them into science- and risk- based approaches
- Have been proven globally (accepted by customers and their regulatory inspectors)
- Are implemented as continuous improvement rather than one-off projects
- Are simple to maintain
- Minimise the impact of change
- Are optimised to address real-life business challenges
- Simplify the addition and removal of products
- Maximise Returns on Investment
For GxP Equipment/Instrument Manufacturers we have developed automated modular commissioning and qualification templates, that can be rapidly populated with existing test details to instantly:
- Provide clear ongoing visibility of validation and compliance status
- Improve product quality and GxP compliance
- Reduce product lead times
- Improve product profitability
- Develop extra revenue streams
- Provide the option of automated Commissioning & Qualification (C&Q) Binder production
- Provide the option of unit fixed cost outsourced C&Q Binder production
Customers
All our products and services are designed to address real business challenges.
Click below to learn how we can assist your organization in resolving the common issues we’ve identified, and facilitate the transition to continuous, science-based, and risk-based validation and compliance.
