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REGULATION (EC) No 726/2004
TITLE I: DEFINITIONS AND SCOPE
TITLE II: AUTHORISATION AND SUPERVISION OF MEDICINAL PRODUCTS FOR HUMAN USE
Chapter 1: Submission and examination of applications — Authorisations
Chapter 2: Supervision and penalties
Chapter 3: Pharmacovigilance
TITLE III: AUTHORISATION AND SUPERVISION OF VETERINARY MEDICINAL PRODUCTS
Chapter 1: Submission and examination of applications — Authorisations
TITLE IV: THE EUROPEAN MEDICINES AGENCY — RESPONSIBILITIES AND ADMINISTRATIVE STRUCTURE
Chapter 1: Tasks of the Agency
Chapter 2: Financial Provisions
Chapter 3: General Provisions governing the Agency
TITLE V: GENERAL AND FINAL PROVISIONS