5
Feb 20
Class I medical device manufacturers may benefit from the transitional period under the MDR
On December 17, a corrigendum to Medical Device Regulation (MDR) 745/2017 was approved by the European Parliament that allows certain devices classified in Class I under Directive 93/42/EEC to benefit from the transitional period provided by the MDR.
24
Oct 19
Ban on the marketing of Cannabis sativa L and its derivatives for recreational use: the ruling of the Unified Divisions of the Supreme Court of Cassation
With Judgment no. 30475 of July 10th, 2019, the Unified Divisions of the Supreme Court of Cassation stated that the marketing of Cannabis sativa L and its derivates (leaves, inflorescences, oil and resin) to the public for recreational use is unlawful unless those derivatives are, in practice, devoid of any doping or psychotropic effect.
3
Jun 19
European Law 2018: amendments to the Drugs Code in regard to the implementation of the GMP
On May 26, 2019, Law No. 37 of May 3, 2019 (“European Law 2018 “) entered into force. Article 16 of this law provides for several amendments to Legislative Decree No. 219 of April 24, 2006 (“The Drugs Code“).
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