Attorney at Work

MAY 18, 2022

Making meetings effective and productive is no easy feat — especially in the age of Zoom. To be effective, meetings need to engage the talents of the people involved, work to achieve the group’s specific goals for the moment — and do so in a way that’s contextually sensitive to the world around it.

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LawSites

JANUARY 17, 2024

Epiq , the global, technology-enabled legal services company, is today launching an antitrust and white-collar compliance product that uses artificial intelligence to help corporate legal departments identify, measure and act on risk within their organizations in real time.

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JURIST

APRIL 26, 2022

The first rule “establishes a revised definition of general lamps” and the second rule “implements the minimum standard of 45 lumens per watt for light bulbs that meet the revised definition.” ” The DOE will host a webinar on May 4, 2022, to field questions from regulated entities.

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Manufacturing 195

Law 360

MARCH 18, 2024

The owner of rights and trademarks of Singer sewing machine products has sued its North American distributor in Delaware's Court of Chancery, seeking a court declaration that it could end their contract because the distributor failed to meet minimum billing and royalties requirements.

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Above The Law

JULY 14, 2022

The growing popularity of cannabis products, combined with the lack of a universal testing protocol, has sprung up the need for testing labs to help meet quality, safety, and labeling requirements for legalized cannabis products.

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FDA Law Blog

MARCH 4, 2024

Livornese — On February 6, 2024, FDA issued a draft guidance titled Notifying FDA of a Discontinuance or Interruption in Manufacturing of Finished Products or Active Pharmaceutical Ingredients Under Section 506C of the FD&C Act. blood supply; and, Manufacturers of certain finished drug products marketed without an approved NDA or ANDA.

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JURIST

JANUARY 18, 2023

Speaking at the World Economic Forum Annual Meeting in Davos, Switzerland, Guterres said, “We learned last week that certain fossil fuel producers were fully aware in the 1970s that their core product was baking our planet.” The WEF annual meeting is taking place from January 16 to 20.

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JURIST

JULY 29, 2021

Described as the “most robust changes to the implementation of the Buy American Act (“the Act”) in almost 70 years,” Biden’s proposal aims to increase US content in the products the federal government buys and support the domestic production of goods and services critical to US national and economic security.

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Manufacturing Small Business Technology Government 211

FDA Law Blog

DECEMBER 15, 2022

By Riëtte van Laack — On December 7, 2022, FDA announced the availability of the final guidance regarding the enforcement policy for homeopathic drug products. FDA concluded that the CPG limited its ability to act against unsafe homeopathic drug products and decided to develop a risk-based enforcement policy.

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LawSites

JANUARY 4, 2024

Now, SpotDraft is releasing the product for general availability, with the option for anyone to try it free for two weeks. I posted a How It Works video demo of that early release version in December, with Rohith Salim , cofounder and chief product officer at SpotDraft. In addition, they have made the product fully self-serve.

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HowAppealing

SEPTEMBER 11, 2023

Chief Justice of Canada concluded a productive two-day meeting with a delegation from the United States Supreme Court last week. Members of the Supreme Court of Canada were delighted to host the Chief Justice of the United States John G.

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Court 100

Paralegal Bootcamp

JUNE 10, 2021

Erik Fisher’s podcast features guests who are experts at everything from virtual meetings, remote management, inbox zero, creativity, and more. How You Can Be Your Best in Virtual Meetings. A SAMPLE OF SOME EPISODES INCLUDE: Health and Productivity Habits. The Productivity Podcast. When People Don’t Support Me.

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LawSites

AUGUST 21, 2023

Relativity Contracts allows users to glean actionable insights when analyzing agreements to meet changing regulatory requirements, realize business value and reduce legal risk,” the company said in its announcement. The product can reduce review time by 40% and enable users to see 50% project cost savings, Relativity said.

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Paralegal Bootcamp

FEBRUARY 17, 2023

Paralegals must effectively communicate with clients and manage their expectations throughout the legal process to maintain a positive and productive relationship. This can be done through regular phone calls, emails, or in-person meetings. Here are some great organization tips. Get 3 Pro Tips for Paralegal Time Management.

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Paralegal Paralegals Immigration Legal 244

iHire

APRIL 1, 2022

Meet your iHire Customer Success Team Member, Lori Cole! Lori leads our Customer Success Team and also plays a key role in new product development.

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JURIST

JUNE 23, 2022

products currently marketed in the US. As a result of the MDOs, JUUL must cease selling and distributing products in the US. In order for a company in the US to legally market a new tobacco product, that company must first receive a written marketing order from the FDA. ” FDA Commissioner Robert M. Califf, M.D.

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FDA Law Blog

MARCH 1, 2023

Richardson — As of the morning of March 1, the hotly anticipated Joint Meeting of the Nonprescription Drugs Advisory Committee and the Anesthetic and Analgesic Drug Products Advisory Committee originally scheduled for March 20 has been cancelled. By Kalie E.

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JURIST

APRIL 30, 2021

The Parliament of Japan (Diet) on Wednesday approved the Regional Comprehensive Economic Partnership (RCEP) free trade deal at a plenary meeting of the House of Councillors (upper chamber of Diet). The agreement aims for the gradual elimination of tariffs on industrial goods and agricultural products.

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FDA Law Blog

APRIL 24, 2024

The meetings have presented a mix of views with some organizations meeting with OMB being in favor of FDA regulation and others being very much opposed. With a final rule now nearly a certainty, a legal challenge seems likely to follow.

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Paralegal Bootcamp

MARCH 9, 2021

MEET & CONFER CHECKLIST FOR LITIGATION PARALEGALS. As a litigation paralegal, part of your case management duties may include getting the attorney ready for the Rule 26 Conference (the “Meet and Confer”). Production. If phasing production, the description of the content each phase. Preservation.

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FDA Law Blog

JUNE 8, 2023

One distinct change has been the rise of conducting meetings over digital platforms. FDA has begun to reintroduce in-person meetings. CDER and CBER CDER and CBER announced they would resume in-person face-to-face (FTF) industry meetings on February 13, 2023. videoconference, teleconference, or an in-person meeting).

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JURIST

NOVEMBER 23, 2023

Unpredictability arises due to a lack of transparency, making it difficult to check whether the model meets standards of quality and accountability. Hallucinations are incorrect outputs that could lead to tort liabilities, consumer harm or regulatory breaches.

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Hoban Law Group

JUNE 8, 2021

If you manufacture, distribute, or sell hemp products in the U.S., you must ensure your products comply with all applicable federal and state labeling regulations. To help sort through these various federal and state requirements, we’ve provided five essential tips for labeling hemp products. Supplement Facts panel); and. (5)

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FDA Law Blog

JULY 11, 2023

Koblitz — One of the most important questions FDA has to answer is whether a given product is appropriately characterized as a drug, biologic, device, food, cosmetic, or something entirely different. As we have explained before , that distinction is critical to assigning a particular product to the appropriate regulatory scheme.

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JURIST

JANUARY 25, 2023

The agreement was reached following a meeting between EU Vice President Maros Šefčovič, UK Foreign Secretary James Cleverly and Northern Ireland Secretary Chris Heaton-Harris. A joint statement released by the parties on January 9 described the meeting as “cordial and constructive.”

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FDA Law Blog

NOVEMBER 2, 2023

It is not especially novel even within CBER, as previous publications had encouraged the use of standards in product development. These meetings have a question-and-answer format to provide clarity to sponsors about the particular topics at hand.

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Customs & International Trade Law

APRIL 2, 2024

Last week, FDA’s Center for Tobacco Products (CTP) announced the release of its Searchable Tobacco Products Database. The FDA has committed to monthly updates, ensuring the availability of current and accurate product information. Provisional Tobacco Products: that have been withdrawn from the FDA review process.

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FDA Law Blog

DECEMBER 20, 2023

For nearly three years following the declaration of the COVID-19 health emergency, there were no in-person meetings held. Then, in early 2023, CDER and CBER started a slow phase-in of in-person meetings in a hybrid format, with some attendees present only virtually. And there we stayed for 6 more months, until now.

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JURIST

JUNE 26, 2021

For example, China subsidized steel to the point where it generated excess steel 65% above demand, which resulted in a worldwide price slump for the product. WTO disputes are heard by the WTO’s Dispute Settlement Body , which meets monthly.

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FDA Law Blog

MARCH 10, 2024

By doing so, FDA/HHS believe that cannabis no longer meets schedule I criteria but does not meet schedule II criteria either. Likely discussion topics during the session will address what has changed since 2016 when FDA/HHS and DEA concluded that cannabis remain in schedule I, why DEA may be required under U.S.

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CARET Legal

APRIL 8, 2024

This intense focus on quantifying productivity through billable targets often leads to overwork, stress, and burnout, with lawyers finding themselves submerged in administrative tasks and complex casework that extends well beyond the conventional workday. It can lead to stress, burnout, and a work-life imbalance.

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FDA Law Blog

MARCH 5, 2023

Koblitz — FDA uses its Product Specific Guidance documents (“PSGs”) to provide recommendations as to the bioequivalence testing necessary for approval of a generic drug. Pre- and post-submission meetings to discuss alternative approaches than that recommended in PSGs may also be available.

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FDA Law Blog

APRIL 30, 2024

Baumhardt, Senior Medical Device Regulation Expert — FDA recently issued a draft guidance on Requests for Feedback and Meetings for Medical Device Submissions: The Q-Submission Program , which included some changes over the existing guidance which could have a negative impact on future pre-submissions.

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Attorney at Work

SEPTEMBER 20, 2022

So I started focusing intently on finding ways to improve my productivity. 5 Attorney Productivity Tips. I experimented with all kinds of productivity “hacks” and most were more trouble than they were worth. Here they are, in case you’re looking for a productivity boost, too. No Meetings on Mondays.

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JURIST

SEPTEMBER 30, 2021

In a statement, Newsom said, This package of smart, bipartisan legislation boosts housing production in California – more streamlining, more local accountability, more affordability, more density. Creating denser housing near jobs, parks and schools is key to meeting our climate goals as well as our affordability goals.

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JURIST

APRIL 9, 2024

Additionally, NATO has established guidance for members’ defense spending of 2 percent of their national Gross Domestic Product (GDP), with more than 66 percent of countries expected to meet this goal in 2024.

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FDA Law Blog

MARCH 26, 2024

Late last week, the FTC submitted an Amicus Brief in recent Hatch-Waxman patent litigation in the District Court of New Jersey between Reference Listed Drug holder Teva Branded Pharmaceutical Products R&D Inc. Because a “drug product” is defined by regulation as a “Finished dosage form. Teva’s patents do not meet that criterion.

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