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Bard operates within a Mundipharma Compliance Framework. We adopt a strategic approach to compliance that is robust for now and for the future. Bard has a Compliance Enrichment Plan that covers

  • Code of Business Ethics
  • Data Privacy and GDPR
  • Data Retention
  • Compliance with the UK Bribery Act
  • Risk Assessments

We adhere to the requirements for Manufacture and Importation of Human Medicinal Products as laid down in directive 2001/83/EC and with the principles of Good Manufacturing Practice (GMP) as laid down in EC Directive 2003/94/EC, as amended respectively, and with the principles and practices set down in the current edition of the Rules Governing Medicinal Products in the European Community, Vol IV, Good Manufacturing Practice (GMP) for Medicinal Products.

We have a proven track record in regulatory compliance that we are very proud of. In recent times our range of Regulatory Audits and Inspections has expanded to include Turkey, Russia, Kenya and China with forthcoming Audits expected from Libya, Uganda and the Beijing FDA.