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Jane Summerfield

Jane Summerfield

Partner
London

Email [email protected]​hoganlovells.com

Phone +44 20 7296 2000

Fax +44 20 7296 2001

LanguagesEnglish

Practice groupGlobal Regulatory

Jane Summerfield is Co-Head of our Life Sciences & Health Care industry sector and leads the Hogan Lovells life sciences regulatory and commercial practice in London. She advises life sciences companies on a wide range of regulatory matters, including clinical trial requirements, early access schemes, marketing authorisations, manufacturing and distribution licences, CE marking, product labelling, advertising and marketing activities, non-promotional activities, and pricing and reimbursement.

Jane also advises on commercial contractual arrangements, including consultancy, sponsorship, co-promotion, collaboration, manufacturing, distribution, services, quality and pharmacovigilance agreements.

Jane works with clients to resolve issues with UK enforcement authorities and regulatory bodies, including the Medicines and Healthcare products Regulatory Agency (MHRA), Prescription Medicines Code of Practice Authority (PMCPA), Advertising Standards Authority (ASA), and Trading Standards.

Jane combines a scientific background with deep regulatory knowledge and a commercial approach, providing "clear responses with business impact" Chambers UK.

Education and admissions

Education

MA Biological Sciences, University of Oxford, New College

PgDL and LPC, BPP University Law School

Bar admissions and qualifications

Solicitor, England and Wales

Related industries

Life Sciences and Health Care

Related practices

Commercial Digital Assets and Blockchain Marketing and Advertising Medical Device and Technology Regulatory Pharmaceuticals and Biotechnology Regulatory Health

Related areas of focus

Advertising and Copy Clearance Agency and Distribution Digital Health False Advertising and Unfair Competition Food and Beverages Food Advertising and Regulation Global Regulatory in the UK Medical Devices Pharmaceuticals and Biotechnology Product Compliance Product Development and Approval Sales Promotions Cell, Tissue, and Gene Therapies Licensing and Commercial Transactions

Representative experience

Advising various multinational pharmaceutical companies on the regulatory requirements relating to marketing authorisations & manufacturing, import & wholesale dealer licences

Advising an international healthcare services provider on the regulatory requirements governing the provision of remote medical services.

Advising a UK pharmaceutical manufacturer on the regulation of the authorisation, pricing and reimbursement, and sale and advertising of medicinal products in the UK.

Advising a U.S. pharmaceutical manufacture on EU & UK SOPs covering approval of marketing materials & activities, hospitality, promotional gifts, samples & medical advisory boards

Advising an internet-based consumer goods retailer on competitor challenges to price claims and a Trading Standards challenge to its on-line ordering process for selling age restricted products.

Advising a leading soft drinks manufacturer on labelling and compositional legislation, advertising copy and defending challenges to products and advertising materials by regulatory authorities.

Advising a UK pharmaceutical company on a co-promotion agreement involving the joint promotion of a new treatment with another major pharmaceutical manufacturer.

Advising a medical device manufacturer on an innovative risk share agreement with a prime contractor supplying services to a Clinical Commissioning Group.

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