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The legislation is now supported with comprehensive Pharmacovigilance modules that Affect Pharmacovigilance; Regulatory; Medical Information; QA; Clinical as well affecting the Senior Management view of Pharmacovigilance requirement and expectations. A Good Pharmacovigilance identifies the risks in the shortest possible time of marketing the drug and will help to establish & identify risk factors. You will be provided with a comprehensive, yet practical assessment of the main Regulations required, in producing a compliant reporting Company.
Trainer: Graeme Ladds Managing Director at Pharsafer, UK
Who should Attend?
This course would be suitable for PV professionals, EU QPPVs, QA & Compliance, Regulatory, Drug Safety, Clinical & Post-marketing, EU and National Regulatory Affairs Officers, Clinical Risk-Benefit Groups, CROs and many interest parties.
For further details please click here.
Article adapted by Medical News Today from original press release. Source:
Please use one of the following formats to cite this article in your essay, paper or report:
Global, Amstad. "EU Pharmacovigilance & Risk Management, 13th & 14th March 2014, Vienna." Medical News Today. MediLexicon, Intl., 25 Nov. 2013. Web.
10 Mar. 2014. <http://www.medicalnewstoday.com/releases/269317>
Global, A. (2013, November 25). "EU Pharmacovigilance & Risk Management, 13th & 14th March 2014, Vienna." Medical News Today. Retrieved from
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