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ServiceUpdated on 22 May 2026

Medical and Scientific Writing

Business Development Lead – EMEA & APAC at DLRC Regulatory Consultancy

London, United Kingdom

About

DLRC consultants, and a team of dedicated medical writers, have considerable experience of medical and scientific writing across a wide range of therapeutic areas and classes of molecules, including non-clinical, clinical and quality aspects. DLRC has a flexible approach, therefore, consultants can write regulatory submissions in their entirety, write documents in collaboration with clients, or provide strategic support and review to clients authoring their own medical and scientific documents.

How can we help?

  • Clinical Trial Documents

  • Clinical Study Reports (CSRs)

  • Global Submission Documents

  • Annual and Safety Reports

  • SOPs and Controlled Documents

Type

  • Consulting

Applies to

  • Biology/Biotechnology
  • Life Science
  • Medicine
  • Therapeutic Area

Organisation

DLRC Regulatory Consultancy

Company

Letchworth Garden City, United Kingdom

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