Specialists in Clinical Trials
Where science, regulation & strategy align for clinical trial success.
Lealto Consulting offers expert regulatory, clinical science, and operational advice and support for early-phase clinical development.
Our Services
About Us
Led by Dr Sally Dowen, Lealto Consulting offers bespoke consultancy services to pharmaceutical and biotechnology companies, contract research organisations (CROs), and clinical research institutions, ensuring tailored solutions for each client’s unique needs.
Recommendations
"I worked with Sally on a complex project and found her help hugely beneficial and impactful.
Sally has pragmatic approach to problem solving using her expert knowledge of the regulations governing clinical trials and clinical investigations of medical devices. We found Sally’s insight into the MHRA and UK Research Ethics Committees extremely useful. Sally is very approachable and felt like she is part of the team with her understanding of our problem and the advice provided!"
Velichka Valcheva, CEO, GH Research
"I have no hesitation in recommending Sally based on her vast experience across all aspects of Clinical Trials, including her experience working within the Clinical Trials section of the MHRA.
Her extensive knowledge from basic science through study design, regulatory affairs and trial implementation provides an excellent background and skillset for her current role as an independent consultant."
Juliet McColm, JR Clinical Research
"Sally is an outstanding clinical trials professional with expert knowledge of all aspects of early phase clinical trials. She’s highly skilled in the scientific and regulatory aspects of early drug development, and has excellent project management, data interpretation and medical writing skills. She achieves excellent results through application of her experience, and knowledge. I thoroughly enjoyed working with Sally – she always brought me solutions not problems."
Kate Darwin, VP Regulatory Affairs, Quotient Sciences
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