Press Releases
Pharmacovigilance, Drug Safety & Risk Management: Novo Nordisk provides expert insight into risk minimisation procedures
LONDON, UNITED KINGDOM - Feb 18, 2015 - SMis 4th annual
Pharmacovigilance, Drug Safety and Risk Management conference will
strengthen knowledge of key Pharmacovigilance issues as well as
navigate through the challenges of compiling PSURs and frequent
safety reports. Understanding legal guidelines, EU harmonisation
initiatives, benefit risk assessments and the analysis of adverse
drug reactions will be a major focus, as will hearing from a
selection of medical bodies and industry KOLS who will be providing
PRAC and Eudravigilance updates.
Highlights this year include an address from Novo
Nordisk Senior Safety Surveillance Advisor, Dr
Kashif Sheikh. The presentation entitled:
Pharmacovigilance management & risk minimisation
procedures to ensure drug safety, will provide unique
insights on drug safety and product life cycle management.
Dr Sheikh will answer questions such as: Can
we strengthen the link between a drug and its related adverse
events from pre-clinical to post-marketing? How do we measure the
effectiveness of risk minimisation activities?
Other Key Speakers Include:
- Jim Slattery, Statistician, Pharmacovigilance, European Medicines Agency (EMA)
- Dr. Tomas Moraleda , International Medical Officer, MedDRA MSSO
- Doris Irene Stenver, Chief Medical Officer, Danish Health and Medicines Authority, Member of PRAC
- Dr. Pipasha Biswas, Executive Director & QPPV, Symogen Ltd
- Dr. Michael Merz, Chair Investigative Liver Expert Team, Novartis Institutes for Biomedical Research
- Shelley Gandhi, Director of Pharmacovigilance and Drug Safety, NDA Group
To download a brochure or for the full speaker line up visit http://www.smi-online.co.uk/goto/2015pharmacovigilance40.asp
In addition to the event, there will be 2 conference workshops taking place on the 13th May 2015 entitled:
- MedDRA Coding Guidelines (Hosted by The International Medical Officer from MedDRA MSSO, Dr Thomas Moraleda)
Targeted towards those involved with coding guidelines and associated standard operating procedures. This workshop will provide an understanding of the scope, structure, and characteristics of MedDRA. The application of the terminology in coding clinical data will also be discussed.
- Risk Minimisation and Signal Management (Hosted by PharSafer Associates CEO, Graeme Ladds)
With an ever increasing focus on monitoring the risk-benefit profile of a product, this workshop will explain the role of safety review, signal detection, risk assessment and risk minimisation in the modern pharmaceutical company.
For those who are interested in attending, there is currently a
£300 discount available which expires on 27th February.
For more information or to register visit
http://www.smi-online.co.uk/goto/2015pharmacovigilance40.asp
Pharmacovigilance, Drug Safety and Risk Management
11th - 12th May 2015
Holiday Inn Regents Park Hotel, London, UK.
http://www.smi-online.co.uk/goto/2015pharmacovigilance40.asp
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About SMi Group:
Established since 1993, the SMi Group is a global event-production
company that specializes in Business-to-Business Conferences,
Workshops, Masterclasses and online Communities. We create and
deliver events in the Defence, Security, Energy, Utilities, Finance
and Pharmaceutical industries. We pride ourselves on having access
to the worlds most forward thinking opinion leaders and
visionaries, allowing us to bring our communities together to
Learn, Engage, Share and Network. More information can be found at
http://www.smi-online.co.uk