ResLabQ&C Ltd
Clinical Research Laboratory
Quality and Compliance
About
ResLabQ&C Ltd was founded in 2020 by Dr Jane Steele, whose vision is to provide highly specialised and expert consultancy services without complexity in a cost efficient and timely manner.
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With a deep understanding and appreciation of the relevant regulatory and scientific frameworks, the services offered by ResLabQ&C are well aligned with activities involving the collection, processing, storage and/or analysis of human biospecimens for translational research studies and clinical trials, for biobanking, and for human application. By offering practical help and advice, we can help you navigate the complex ethical, legal, and regulatory landscape and enable you to operate compliantly to the quality standards expected, ensuring participant confidentiality and assuring the reliability, quality, and integrity of the data you produce.
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We can work with you at any phase of your project; during the set-up of a new facility or study; whenever the development and implementation of systems that drive improvement in quality and compliance become necessary; or to provide practical and efficient solutions when specific issues arise at any time. We recognise that each facility or institution has unique needs and tailor services to provide client-specific solutions. The highest ethical and confidentiality standards are maintained at all times.
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If you require current, on-demand regulatory support tailored directly to you, please contact us to discuss how we can help.
Dr Jane Steele - Founder
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Jane Steele has an academic research background in viral immunology and hands-on experience of delivering the laboratory aspects of early phase clinical trials. She has spent the last 12 years working at Directorship level at the University of Birmingham where she was responsible for the establishment and oversight of a large HTA-licensed ethically approved Research Tissue Bank, and subsequently of an adjacent facility manufacturing cell- and tissue-based therapies administered to patients both on and off clinical trial.
Jane has extensive experience of regulatory compliance within clinical research laboratories and a detailed understanding of the NHS environment with respect to clinical research. She has been responsible for the successful delivery of multiple complex projects concurrently, and for developing strong collaborations with a diverse group of stakeholders, internal staff, contract teams, clinical research communities, commercial organisations, and regulatory bodies. She has established ResLabQ&C Ltd in order to use her knowledge and experience to deliver regulatory services and guide the creation and implementation of effective Quality Management.