Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relates to medicinal products for human use in mainly countries that are part of the European Union.[1] The Directive dealt with the disparities between certain national provisions, in particular between provisions relating to medicinal products, which directly affected the functioning of the internal market of the European Union.

See also

References

  1. "EUR-Lex - 32001L0083 - EN". Official Journal L 311. 28 November 2001. pp. 67–128. Archived from the original on 25 January 2022. Retrieved 2022-02-26.
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