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Bär & Karrer | Switzerland, Global | 29 Apr 2019

Clinical trials in Switzerland

A structured guide to clinical trials in Switzerland


Mattos Filho Veiga Filho Marrey Jr e Quiroga Advogados | Brazil, Global | 2 Apr 2019

Collection, storage and transfer of data in Brazil

A structured guide to the collection, storage and transfer of data in Brazil


Gowling WLG | Canada | 27 Jan 2019

Le commissaire à la protection de la vie privée exige la révision des politiques de confidentialité

Je consens (sous réserve de ce que le commissaire à la protection de la vie privée juge valable) : feuille de


OLIVARES | Mexico, Global | 8 Jan 2019

Clinical trials in Mexico

A structured guide to clinical trials in Mexico


CMS Belgium | Belgium | 5 Dec 2018

Important legal changes in Belgium's healthcare sector

A new law was adopted on 30 October 2018 containing various provisions on health. This law contains amendments to different regulations in the


Baker McKenzie | USA | 30 Nov 2018

Negative Option Billing Enforcement Actions, False Advertising, and Endorsements

The Federal Trade Commission (FTC) continues to bring enforcement actions against companies that engage in false advertising and deceptively enrolling


Troutman Sanders LLP | Global | 20 Nov 2018

Solving The Mystery Of Contracting By Hyperlink

Remote contracting with customers through the internet is either the current reality or the aspirational goal for many businesses. This article


Epstein Becker Green | USA | 20 Nov 2018

FDA Loosens the Reins on Informed Consent Requirements for Certain Clinical Studies

Following up on its July 2017 guidance on the same topic (discussed in a previous blog post), FDA issued a proposed rule on November 15, 2018 to


Baker & Hostetler LLP | USA | 19 Nov 2018

BakerHostetler FDA and Pharmacy Weekly Digest - November 19, 2018

The Food Safety Analytics Collaboration released a new report titled “Foodborne illness source attribution estimates for 2016 for Salmonella


Dinsmore & Shohl LLP | USA | 15 Nov 2018

FDA Proposes Changes to Clinical Trial Informed Consent Rules

On November 15, 2018, the Food and Drug Administration (FDA) published a Proposed Rule, which, if finalized, will allow an institutional review board

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