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20 Dec 2023, 2:50 pm by Cynthia Marcotte Stamer
They also made sexual comments about female employees, critiquing their physical appearance and referring to the employees’ personal relationships. [read post]
20 Dec 2023, 1:01 pm by Gene Takagi
The proposed regulations would provide that facts and circumstances that are relevant in determining that a fund or account is separately identified by reference to contributions of a donor or donors include: (1) the fund or account balance reflects items such as contributions, dividends, interest, distributions, administrative expenses, and gains and losses (realized or unrealized); (2) the fund or account is named after one or more donors, donor-advisors, or related persons; (3) the… [read post]
19 Dec 2023, 4:48 pm by Cynthia Marcotte Stamer
This extension will be provided automatically and does not require a request by disputing parties. [read post]
But at what point does all that tech do more harm than good? [read post]
19 Dec 2023, 12:00 am by admin
However, a critical point is that S4516 does not modify Section 5003-B of the CPLR. [read post]
Also, in contrast to bereavement leave, this category of leave does not require a written request or any sort of proof as a prerequisite to granting this leave. [read post]
15 Dec 2023, 12:17 pm by Josh Blackman
Disclosure #5: Justice Kavanaugh's relisted Dobbs to kick it till the next term Had the Court granted Dobbs at the first conference in January 2021, the case would have likely been hard at the end of April 2021, with a decision by June 2021. [read post]
13 Dec 2023, 7:47 am by Joel R. Brandes
 December 6, 2023   A court cannot reform an agreement to conform to what it thinks is proper, if the parties have not assented to such a reformation. [read post]
12 Dec 2023, 8:33 pm by Yosi Yahoudai
The post What is the FMCSA and how does it affect truck drivers? [read post]
11 Dec 2023, 8:33 pm by Kurt R. Karst
Even using a lower, out-of-date number of laboratories, FDA anticipates receiving an astounding number of premarket review submissions for LDTs, specifically: 32,160 510(k) premarket notifications; 4,210 PMAs, PDPs, Panel-Track PMA Supplements; and 4,020 de novo[4] FDA derives these estimates by applying the same metrics applicable to currently‑regulated IVDs: 50% undergo premarket review, and of those 40% are submitted through the 510(k) process, 5% are submitted for de novo… [read post]