Pharma R&D Today
Ideas and Insight supporting all stages of Drug Discovery & Development
Senior Solution Marketing Manager
About the author:
As a Senior Solution Marketing Manager at Elsevier, Sherry is responsible for delivering insights on markets and customers, messaging, positioning and thought leadership for life science solutions, including PharmaPendium, that enable Drug Discovery and Development and Pharmacovigilance.
Sherry has a PhD in Medical Genetics from the University of Toronto, Canada and has several years of experience in life science marketing and communications, having worked at QIAGEN in Hilden, Germany before joining Elsevier and also in Research Communications at the University Health Network in Toronto, Canada. Prior to this, Sherry performed research at cancer institutes in both Canada and the US.
Posts by Sherry Winter
Posted on September 29th, 2017 in Pharma R&D
Widespread underreporting is often cited as a factor that curtails the analytical value of data from spontaneous reporting systems. Voluntary submission of reports is a core feature of these systems but it also means that not all events suspected to be associated with a medicinal product are documented and brought to the attention of authorities and marketing authorization holders – (more…)
Posted on September 25th, 2017 in Pharma R&D
In 2012, the U.S. Food and Drug Administration (FDA) provided draft guidance for the industry on drug interaction studies, stating that “pharmacokinetic interactions between an investigational new drug and other drugs should be defined during drug development, as part of an adequate assessment of the drug’s safety and effectiveness.” (more…)
Posted on September 13th, 2017 in Pharmacovigilance
Pharmacovigilance is essential to pharmaceutical businesses. It facilitates the correct use of a drug, safeguarding the drug as a meaningful treatment option when the benefits it offers outweigh known risks, or measures can be taken to mitigate those risks. (more…)
Posted on August 9th, 2017 in Pharmacovigilance
In their 2012 Drug Regulations, the U.S. Food and Drug Administration recommended that “pharmacokinetic interactions between an investigational new drug and other drugs should be defined during drug development.”