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Cécile Derycke

Partner
Paris

Cécile Derycke

Passionate about litigation and human beings, Cécile Derycke has grown a practice focused on disputes in the life sciences area. Cécile coordinates our Paris life sciences practice and is the Co-Head of our global Life Sciences Litigation Arbitration & Employment Team. She handles product liability cases, commercial litigation matters and various contentious situations regarding regulatory requirements. Cécile joined Hogan Lovells more than thirteen years ago as a general litigator and product liability lawyer.

Hand in hand with our regulatory team, she has built the Life Sciences practice of our Paris office. Cécile handles many different types of contentious issues for companies in the life sciences sector. She has particular experience in multi-jurisdiction bodily injury cases and the cross-border coordination of such cases. She is handling the largest product liability case ever brought before the French civil courts in terms of number of plaintiffs. Cécile works every day on complex legal, procedural and media issues raised by such matters.

She has also developed a very sharp understanding of the class actions mechanisms which are spreading over Europe, including France. Cécile's close connections with our regulatory team and her deep knowledge of the life sciences industry have also made her a key player in litigious matters involving regulatory issues. She very often advises our clients on their interactions with the health authorities regarding pricing and reimbursement, product safety, etc. She also works on complicated promotional subjects either raised by the authorities or by competitors.

'Clients praise her “strategic thinking” and “commanding presence in court''

Who's Who Legal Life Sciences 2015

Representative Experience

Defense of TÜV Rheinland against liability claims resulting from allegedly inappropriate certification of breast implant manufacturer P.I.P.

We represent a pharmaceutical company in litigation against the French Economic Committee for Health Products ('CEPS') regarding the price conditions of an orphan drug.

We advise a medical devices manufacturer on an inspection regarding materiovigilance carried out by the French health authorities and the follow up actions.

We assist a pharmaceutical company in investigating a product safety issue and assessing claims against an excipient supplier and of clients.

We assist a medical device manufacturer in the context of administrative investigations, criminal and civil proceedings relating to the over-irradation of patients.

We represent orthopaedic medical devices manufacturers in unfair competition matters relating to the alleged poaching of sales representatives, in particular.

Education and admissions

Education

  • D.E.S.S., Université Paris II, Panthéon-Assas, 2002
  • DJCE, Université Paris II, Panthéon-Assas, 2002
  • Magistère Juriste d’affaires, Université Paris II, Panthéon-Assas, 2002

Memberships

  • European Leadership Council
  • DRI International

Bar admissions and qualifications

  • Paris

2015

Band 1 (Paris Life Sciences Group) – Legal 500 EMEA

2015

Acclaimed internationally for her work defending product liability claims – Who's Who Legal

2014

Shortlisted for 'Best in Life Sciences'

Euromoney European Women in Business Law Awards

2014

Notable expertise in healthcare-related cases

Legal 500 EMEA

2013

Recommended for sensitive cases relating to pharmaceuticals and medical devices

Legal 500 EMEA

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