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C5 - 3rd EU Pharma Law & Regulation Conference

Event

2012 is set to be a critical year for EU pharma regulation with the implementation of the pharmacovigilance rules, proposals to amend the data protection and clinical trials directives and the new falsified medicinal products directive.


In addition, the Mediator case triggered an overhaul of regulation governing the healthcare sector in France and a drive towards increased transparency and the impact of this case is likely to be felt across the EU.


Questions are being raised about anti-corruption efforts and where we are a year on from the introduction of the UK Bribery Act.


There are a number of competition law developments, there are concerns regarding off-label promotion and a number of legal problems are arising as a result of pharma companies developing their social media presence.


The budgetary pressures across Europe and the Eurocrisis are having a critical impact on health authorities across Europe and the scope of SPCs has been clarified.


Werner Berg is speaking on the topic, "How to Align Your Business Practices in Light of Recent Competition Law Judgments."

Insights

Event | 12.04.25

ACI 30th Annual Conference on Drug & Medical Device Litigation

Dan Campbell with Speak on the panel "Mastering MDL Case Management: What Proposed Rule 16.1 Really Means for Consolidated Litigation."
Rule 16.1 attempts to guide early case management in MDLs, impacting litigation pace and costs. Permissive language like “should” instead of “must”, could lead to inconsistent applications. This panel will explore the rule’s anticipated impact and implications for procedures.