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Depositions in shorts after the pandemic? Remote depositions are likely becoming the norm, but dress-down shouldn't | Farrell Fritz, P.C.


(see
Fed. R. Civ. P. 30(b)(4)).  The dramatic increase in use, comfort level, and apparent permanency is a direct result of the pandemic. Indeed, the vision of the Commercial Division Advisory Council (“CDAC”) is to ensure that the Commercial Division remains at the forefront of this trend.
In September 2020, the CDAC sought to adopt a new Commercial Division Rule that would expressly authorize and regulate the use of remote depositions (the “
Remote Deposition Proposal”).  The Remote Deposition Proposal seeks to provide further guidance on what is considered undue hardship, a standardized remote deposition protocol form, the validity of an oath or affirmation administered during a remote deposition when the court reporter is not physically located where the witness is present, and protections for defending attorneys and their clients in the event of technical difficulties.  The Proposal went out for ....

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30(b)(6) Discovery in the Age of COVID-19 | Rumberger | Kirk


Defending corporate representative depositions in the new reality.
If there is one lesson all trial lawyers have learned over the last year, it’s that life and the practice of law must go on, even in the face of upheavals affecting our profession. Depositions of corporate representative witnesses under Rule 30(b)(6), Federal Rules of Civil Procedure is a prime example of how lawyersmust learn to adapt to changing times and circumstances.
Rule 30(b)(6) of the Federal Rules of Civil Procedure, along with its state equivalents, has become an integral part of trial practice defending corporations. The Coronavirus pandemic, however, has caused dramatic changes in practice under this Rule, along with alterations in many other aspects of law practice. These changes are all too familiar to most trial counsel, and need not be discussed in detail here. ....

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Plaintiff Alleges Hip Implant Caused Heightened Levels of Metals in Bloodstream in Suit Against DePuy


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January 26, 2021
On Monday in the Northern District of Texas, two individuals filed a complaint against DePuy Orthopaedics Inc., Johnson & Johnson, and affiliated entities that claimed that the defendants knowingly continue to manufacture, market, and sell a hip implant device that allegedly caused harm, in the form of “debilitating pain” and increased blood levels of certain metals.
The medical device in question, called the pinnacle device, is a Class III hip implant, which means it “operates to sustain human life, (is) of substantial importance in preventing impairment of human health, or pose(s) potentially unreasonable risks to patients,” according to the complaint. Class III devices generally have to undergo a rigorous premarket approval process by the Food and Drug Administration (FDA) to thoroughly vet a product for safety and efficacy, pursuant to the 1976 Medical Device Amendments (MDA) to the Food, Drug, and Cosmetics Act. ....

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