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Paul Ranson

Consultant Solicitor

England & Wales

020 3319 3700

paul.ranson@keystonelaw.co.uk

An accomplished regulatory life sciences expert, Paul has 30 years’ experience and expert knowledge of the regulatory, commercial, intellectual property, and product liability needs of the pharmaceutical, biotechnology, and medical device sectors on an international and domestic scale. Clients have included leading pharmaceutical companies such as Smith Kline Beecham.

Expertise

Paul advises on the regulatory, commercial, intellectual property and product liability needs of the pharmaceutical, biotechnology, and medical device sectors on an international and domestic scale.

Experience

  • Acted in 20 major product acquisitions for various clients.
  • Acted for Antisoma in what was then the largest licensing biotech deal in the UK with Roche.
  • Advised on various co-development agreements with biotechnology companies and big pharma including Apitope and Merck Serono.
  • Provided European regulatory support for multi-billion-dollar/pound worldwide deals including for companies such as GE Healthcare and BTG.
  • Overhauled the clinical development contracting structure for various multinationals.

Please note: The experience list above may include examples of work completed prior to joining Keystone Law.

Recognition

Recognised by Best Lawyers (UK) for Life Sciences Law 2020–2025

Recognised by The Legal 500 for Corporate and Commercial: Venture Capital 2023

“At the ‘excellent’ Keystone Law, commercial and regulatory lawyer Paul Ransom joined from Pinsent Masons LLP in May 2015”

The Legal 500 2016

Paul qualified as a solicitor in 1986 and as a barrister in 1975. Prior to joining Keystone Law in 2015, he worked at the following firms:

  • Pinsent Masons
  • Fasken Martineau
  • Simmons & Simmons