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Clinical Trials & REMS in the Time of Corona: FDA & MHRA Advice and Guidance
Pharmacovigilance expert Bart Cobert discusses the FDA and MHRA guidance for non-Corona related clinical trials.
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Does Rapid FDA Approval Produce Drug Safety Issues?
Bart Cobert gives his pharmacovigilance point of view on a recent paper on FDA approval timelines and drug safety issues.
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Clintrials.gov Update
Bart Cobert on the importance of publishing clinical trials data and implications on pharmacovigilance.
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Pharmacovigilance 2030
This is an interesting article looking at what PV will be in the year 2030.
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FDA Draft Guidance on PMRs
Bart Cobert highlights the most important changes in the recently revised FDA draft guidance on PMRs.
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Ranitidine – What Happened and What Do We Learn?
Bart Cobert explores several important points to take from the still ongoing signal and safety issue with Renitidine recall.
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Video Email: Your Secret Weapon in Improving cSat
The advantages of utilizing video email response to overcome low customer satisfaction.
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Why Coupons Are Still a Powerful Strategy for Brands
When it comes to driving consumer behavior, coupons continue to be a powerful force.
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Going Mobile: Creating Experiences that Matter with the Avaya Mobile Experience
Read how C3i Solutions is leveraging Avaya Mobile Experience to provide better customer experience.
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Vaping – A Serious Safety Signal
Bart Cobert discusses the major safety issue in the US on e-cigarettes and vaping.
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