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SFL Regulatory Affairs & Scientific Communication Ltd.
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Pharmacovigilance & Clinical Safety

Support safety management throughout product lifecycle.

SFL’s Pharmacovigilance team has long-standing experience in EU and Swiss pharmacovigilance processes and supports headquarter companies and their affiliates in achieving pharmacovigilance excellence in compliance with good pharmacovigilance practice (GVP) regulations. SFL team members can act as EU Qualified Person Pharmacovigilance (QPPV) and local QPPV, conduct gap analyses and PV audits, and set-up PV Quality Systems and Pharmacovigilance System Master Files (PSMF).

  • Services

  • Regulatory Affairs
  • Quality Assurance & GxP Compliance
  • Medical Affairs & Communication
  • Market Access & Reimbursement
  • Public Affairs & Regulatory Intelligence
  • Medical Devices, Combination Products and IVDs
  • Pharmacovigilance & Clinical Safety
  • Supply Chains of Medicines and Devices
  • Legal & Healthcare Compliance
  • Swiss Support
  • UK Support
  • Clinical Trials support

Switzerland – Main Office

SFL Regulatory Affairs & Scientific Communication GmbH
Aeschenvorstadt 52 | CH-4051 Basel
Email: office@sfl-services.com
Phone: +41 61 361 9443

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