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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
