Event : Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance http://www.rsc.org/events/detail/10239/Writing%20Effective%20Clinical%20Evaluation%20Reports%20as%20Part%20of%20Post-Market%20Surveillance This is a feed for event : Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance Thu, 11 Sep 2014 13:13:13 +0100 10239 10239 http://www.rsc.org/events/detail/10239/Writing%20Effective%20Clinical%20Evaluation%20Reports%20as%20Part%20of%20Post-Market%20Surveillance Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance Event dates: 24 January 2014<br/>Event summary: This medical device webinar will discuss strategies for meeting the Post Market Surveillance requirements as described in Annex X of the MDD (MDD 93/42/EEC, updated per the 2007/47/EEC M5 amendment,<br/>Event Venue: Online Event, Palo Alto, 94303, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00