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Our validation-in-a-box framework
Converting to Thermo Scientific culture media
Whether you are in the Pharmaceutical, Biotechnology, or BioPharma industry, our validation-in-a-box framework empowers microbiology labs to transition from existing protocols to new, improved ones seamlessly. From the validation protocol drafting, to the successful implementation of routine practices, we are here to support you every step of the way.
Why choose Thermo Fisher Scientific?
For over 100 years, we have empowered laboratories by providing expert advice, guidance, support, and the tools needed to deliver exceptional results worldwide.
Using this experience, we have developed the validation-in-a-box framework to guide you through the media supplier conversion process step by step, providing the tools you need to successfully manage your transition, tips from our recognised experts on what to expect when converting, administrational documentation, and hands-on support. Our focus is reducing the burden of transitioning to Thermo Fisher Scientific as your new media supplier.
Experience a streamlined transition, unparalleled support, and a commitment to exceptional quality. Contact us today to learn how Thermo Fisher Scientific can empower your lab's success.
Microbiologists supporting microbiologists
At Thermo Fisher Scientific, we understand the unique needs of microbiology labs. Our experienced technical support team collaborates closely with customers, prioritising each product conversion and ensuring comprehensive quality testing and documentation. Through a thorough audit, we identify the most suitable solutions and alternatives, gather the necessary certificates, and establish communication with manufacturing to ensure a seamless supply chain.
Every step of the way
Even after the conversion process, Thermo Fisher Scientific remains committed to providing ongoing support to optimise your new techniques and enhance your lab's efficiency. We are dedicated to continuous improvement, constantly generating innovative ideas to overcome everyday challenges. Our unparalleled service covers protocol assistance, product transitions and troubleshooting.
The media conversion process
Here's an overview of the steps involved in the validation-in-a-box media conversion process, to learn more download the infographic.
- Cross-reference
- Supply booklet
- Evaluation
- Review
- Sustainability
Our team provides a complete list of alternatives in accordance with the cross-reference checklist.
The "Validation-in-a-Box" supply booklet contains all the material to support practical works, documentation and certification needs.
The technical team will develop a support framework your validation works, timelines, and plan for support training.
Review of results and acceptance criteria, followed by an onboarding inventory worksheet and local handover.
Post-adoption review and roadmap for continual improvement.
More than just documentation
We understand the challenges in transitioning to a new media supplier, and our focus is reducing the burden for you. Throughout the validation-in-a-box conversion process, our technical support team works alongside you, providing assistance in drafting the validation protocol and supporting its implementation in your routine work. We offer comprehensive materials and documentation to facilitate a seamless transition.
Quality is more than a process; it's a passion
At Thermo Fisher Scientific, we are driven by a passion for quality. We adhere to strict quality standards, from testing raw materials to maintaining temperature control. Our state-of-the-art microbiology manufacturing facilities operate under Quality Management Systems compliant with ISO 13485 and 9001. Additionally, our prepared media manufacturing laboratories in Adelaide, Australia; Perth, U.K.; and Wesel, Germany, hold accreditation to ISO 17025.