{"id":20259,"date":"2024-02-08T14:54:09","date_gmt":"2024-02-08T14:54:09","guid":{"rendered":"https:\/\/dponl.server.terryh.uk\/?post_type=avg&p=20259"},"modified":"2024-02-08T14:54:10","modified_gmt":"2024-02-08T14:54:10","slug":"overweging-161","status":"publish","type":"avg","link":"https:\/\/www.dpocentre.nl\/en\/bronnen\/avg\/overweging-161\/","title":{"rendered":"Overweging 161"},"content":{"rendered":"

Wat betreft de toestemming voor deelname aan wetenschappelijke onderzoeksactiviteiten in klinische proeven dienen de desbetreffende bepalingen van Verordening (EU) nr. 536\/2014 van het Europees Parlement en de Raad van toepassing te 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