# Commission Implementing Regulation (EU) No 520/2012 of 19 June 2012 on the performance of pharmacovigilance activities provided for in Regulation (EC) No 726/2004 of the European Parliament and of the Council and Directive 2001/83/EC of the European Parliament and of the Council (Text with EEA relevance), Division 5

Extent: E+W+S+N.I.

Milestones: dates for the following milestones:
(a)start of data collection (planned and actual dates);
(b)end of data collection (planned and actual dates);
(c)study progress reports;
(d)interim reports of study results, where applicable;
(e)final report of study results (planned and actual date);
(f)any other important milestone applicable to the study, including date of study registration in the electronic study register.

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Source: https://www.legislation.gov.uk/eur/2012/520/annex/III/division/3/division/5 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-520/annex-III/division-3/division-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.