On June 4, 2021, the European Commission adopted a new, highly anticipated set of standard contractual clauses to facilitate the transfer of personal data out of the European Economic Area (“EEA”) in accordance with the...more
9/20/2021
/ Corporate Counsel ,
EU ,
EU Data Protection Laws ,
European Commission ,
European Economic Area (EEA) ,
Information Commissioner's Office (ICO) ,
International Data Transfers ,
Personal Data ,
Popular ,
Privacy Laws ,
UK
On March 26, 2020, Tennessee Governor Bill Lee signed Executive Order No. 20, with immediate effect. Executive Order No. 20 amended and significantly expanded the health care specific sections of Executive Order No. 15,...more
4/2/2020
/ Certificate of Need ,
Coronavirus/COVID-19 ,
Executive Orders ,
Governor Lee ,
Health Care Providers ,
Healthcare Facilities ,
Healthcare Workers ,
Licensing Rules ,
Relief Measures ,
State of Emergency ,
Telemedicine
On March 19, 2020, the Mississippi Department of Health (“MSDH”) issued a press release advising that “elective medical procedures and non-essential medical visits must be postponed.” (emphasis added). (See...more
On March 13, 2020, the Tennessee Board of Licensing of Health Care Facilities issued Policy Memorandum #82 entitled “Interpretation and Temporary Waiver of Rules Related to Treatment and Containment Of COVID-19”. Policy...more
It’s hard to believe a decade has passed since we delivered our first edition of Pro Te: Solutio to your door. Those years have brought enormous changes in the world and in our industry. Innovation has driven everything we...more
7/17/2018
/ 21st Century Cures Act ,
Affordable Care Act ,
Client Services ,
Depositions ,
DQSA ,
Emergency Response ,
Enforcement Actions ,
FDASIA ,
Food and Drug Administration (FDA) ,
Food and Drug Administration Amendments Act (FDAAA) ,
Health Care Providers ,
Health Insurance ,
Hospitals ,
Innovation ,
Juror ,
Jury Trial ,
Law Firm Associates ,
Law Firm Ownership ,
Law Firm Partners ,
Law Practice Management ,
Manufacturers ,
Medical Device User Fee Program (MDUFA IV) ,
Medical Devices ,
Multidistrict Litigation ,
Patient Rights ,
Patient Safety ,
Patients ,
Pharmaceutical Industry ,
Preemption ,
Questionnaires ,
Reporting Requirements ,
State Law Tort Claims ,
Voir Dire ,
Witness Preparation
The Fall 2016 issue of Pro Te is about all things regulatory, including a peek at the newly developing issue of crowdfunding for medical devices.
In EMA Guidance on Clinical Data Publication, we discuss recent guidance...more