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Lisa Page

Dr Lisa Page is a partner in the intellectual property team in Birmingham who specialises in the life sciences sector. With a client base ranging from pharmaceutical companies to biotech start-ups and spin-outs, she advises on all stages of the drug development pathway including registration, regulatory, pharmacovigilance, pre-clinical and clinical development as well as on multi-party collaborations and spin-outs. She has particular experience in the development stage of new products, covering pipeline, co-development, out-licensing and in-licensing arrangements. Alongside intellectual property and life sciences, Lisa has a separate practice focusing on state aid as it applies to research and development including the R&D&I Framework and GBER. She has advised on a number of high value grant funded and research infrastructure projects in addition to providing guidance to research organisations more generally on state aid compliance. Lisa has a PhD in molecular microbiology and direct practical experience of working in the pharmaceutical industry before re-training as a solicitor. Her scientific background provides a specialist insight into the issues faced by her clients and enables her to speak their language when advising on development programmes and the exploitation of life science technologies. She has held a number of in-house legal roles, including at the Energy Technologies Institute and Coventry University. · Penningtons Manches Cooper LLP

EnglandIntellectual Property, Life Sciences

About

Partner in the intellectual property team in Birmingham specialising in the life sciences sector, advising pharmaceutical companies and biotech start-ups across the drug development pathway (registration, regulatory, pharmacovigilance, pre-clinical and clinical development), and on multi-party collaborations, co-development and licensing. Also advises on state aid for research and development (including the R&D&I Framework and GBER); holds a PhD in molecular microbiology and has prior pharmaceutical industry and in-house legal experience.

Practice areas

Intellectual PropertyLife SciencesRegulatoryState AidEducation

Office

Expertise

PharmaceuticalsBiotechnology start-ups and spin-outsDrug development (registration, regulatory, pharmacovigilance, pre-clinical & clinical)Co-development, out-licensing and in-licensing arrangementsGrant-funded projects and research infrastructureAdvice to research organisations and universities

Education

  • PhD in Molecular Microbiology