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DIRECTIVE 2001/83/EC
TITLE III: PLACING ON THE MARKET
Chapter 1: Marketing authorization
Chapter 2: Specific provisions applicable to homeopathic medicinal products
Chapter 2A: Specific provisions applicable to traditional herbal medicinal products
Chapter 3: Procedures relevant to the marketing authorization
TITLE IV: MANUFACTURE AND IMPORTATION
TITLE V: MANUFACTURE AND IMPORTATION
TITLE VI: LABELLING AND PACKAGE LEAFLET
TITLE VII: WHOLESALE DISTRIBUTION AND BROKERING OF MEDICINAL PRODUCTS
TITLE VIIA: SALE AT A DISTANCE TO THE PUBLIC
TITLE VIIIA: INFORMATION AND ADVERTISING
TITLE IX: PHARMACOVIGILANCE
CHAPTER 1: General provisions
CHAPTER 2: Transparency and communications
CHAPTER 3: Recording, reporting and assessment of pharmacovigilance data
CHAPTER 4: Supervision of post-authorisation safety studies
CHAPTER 5: Implementation, Delegation and Guidance
TITLE X: SPECIAL PROVISIONS ON MEDICINAL PRODUCTS DERIVED FROM HUMAN BLOOD AND PLASMA
TITLE XI: SUPERVISION AND SANCTIONS
TITLE XII: STANDING COMMITTEE
TITLE XIII: GENERAL PROVISIONS
TITLE XIV: FINAL PROVISIONS