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Strong laws of large numbers for weighted sums of ????-dimensional arrays of random variables and applications to marked point processes

Ta Cong Son, Tran Manh Cuong, Le Quang Dung and Le Van Dung
Theor. Probability and Math. Statist. 111 (), 153-165.
Abstract, references and article information




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Trial Set for 2020 in Long-Running Pennsylvania School Funding Lawsuit

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Reading Instruction: A Flurry of New State Laws

Many states have recently enacted laws or rules designed to ensure that teachers are well versed in evidence-based reading instruction. Here are some highlights.




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Ohio Supreme Court dismisses Toledo bullying lawsuit




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Wyoming, Idaho Laws Expand K-12 Computer Science Education

All districts in Wyoming will be required to provide K-12 computer science instruction, and Idaho high schools will offer at least one high school CS course.




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Ohio Supreme Court dismisses Toledo bullying lawsuit




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New Virginia laws seek to close ‘school-to-prison pipeline’




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Lawsuits Defy Arizona Initiative Taxing Wealthy for Schools

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New Virginia laws seek to close ‘school-to-prison pipeline’




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Rural Districts in New Jersey Lose Funding Lawsuit

The lawsuit alleged that rural districts in the state have been underfunded for years.




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Hawaii Settles Lawsuit on Illegal Age Limit for Special Education

About $8 million will be eligible for compensatory education to students who were affected by an illegal state-imposed age cap on special education enrollment.




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Federal Judge Dismisses Most Claims in Connecticut School Choice Lawsuit

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Connecticut Supreme Court OKs Part of Newtown Parents' Gun Industry Lawsuit

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Lawsuit Challenges Florida's Post-Parkland Plan to Arm Some School Employees

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Vote to Dissolve Little Rock, Ark., School Board Results in Lawsuit

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New laws for drink driving and drug driving

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Advocates welcome promised pay equity laws in N.B., but warn some will be left out

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'Financially desperate' Winnipeg business swindled out of 2 properties, lawsuit alleges

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Syilx Okanagan woman files lawsuit alleging historic abuse at Vernon Catholic school

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Autodesk, Inc. and Dassault Systèmes SolidWorks Corp. Settle Lawsuit




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App Store faces Epic Games-style antitrust lawsuit from Chinese developer

The developer of an app dropped from the App Store in China has filed a lawsuit that challenges Apple's overall practices, as well as damages of $420,000.


China and the App Store

Apple has consistently been bowing to pressures from China and dropping apps from the App Store in the region. In this case, it's claimed an app called Bodyreader was pulled by Apple over reasons the developer believes are inconsistent.

According to Bloomberg Beijing's intellectual property court has accepted a complaint from Bodyreader's developer. The publication describes this as an Epic Games-style lawsuit on account of its scope concerning Apple's overall practices on the App Store.


Continue Reading on AppleInsider | Discuss on our Forums




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'This Road Just Got a Lot Harder': Teachers' Unions Hit With New Round of Lawsuits

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Judge Dismisses Concussion Lawsuit Against Illinois High School Association

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Judge Allows Lawsuit Against Pop Warner to Proceed to Trial

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Ohio Supreme Court dismisses Toledo bullying lawsuit




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Schools Seek Cover From Special Education Lawsuits, But Advocates See Another Motive

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Schools Seek Cover From Special Education Lawsuits, But Advocates See Another Motive

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Contest explores artificial intelligence’s strengths, flaws for medical diagnoses

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Ask an expert: Harris 2024? Here’s what election and campaign finance laws say

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News24 Business | Lindt melted own 'excellence' claim in US lawsuit: reports

In a bid to dodge a US lawsuit, Swiss chocolatier Lindt & Sprungli has scuppered its own claims about the excellence of its products — a cornerstone of its marketing strategy.




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AG Jennings Announces Lawsuit To End Google’s Illegal Monopoly

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  • Attorney General Kathy Jennings
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AG Jennings Announces Lawsuit Against Seaford

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AG Jennings Wins Seaford Lawsuit

Chancery ruling invalidates illegal fetal tissue ordinance A fetal tissue ordinance enacted by Seaford City Council late last year has been overturned following a successful legal challenge by Attorney General Kathy Jennings and the Delaware Department of Justice. The ordinance, enacted on December 14 with an original effective date of January 22, would have forced […]



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Jennings, AGs, and Advocates Announce Proposed Settlement in Chesapeake Pollution Lawsuit

Attorney General Kathy Jennings and her colleagues have announced that a proposed settlement has been reached in the 2020 lawsuit against the Environmental Protection Agency (EPA) for its failure to require Pennsylvania to develop and implement a plan to meet its commitments to reduce pollution under the Chesapeake Clean Water Blueprint. One-third of Delaware is […]



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AG Jennings’ Statement On Prehired lawsuit

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AG Jennings files lawsuit against chemical companies for causing contamination of Delaware’s natural resources

Attorney General seeks damages, including costs necessary to restore impacted natural resources and funding for State-run public health programs. Attorney General Kathleen Jennings announced that the Department of Justice has filed a lawsuit to hold numerous companies accountable for contaminating Delaware’s natural resources with per- and poly-fluoroalkyl substances (PFAS) traceable to the use and disposal […]



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Gulf region loosens foreign investment laws

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The physicist who argues that there are no objective laws of physics

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The physicist who argues that there are no objective laws of physics

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The laws of physics appear to follow a mysterious mathematical pattern

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Mandatory Life Jacket Laws Could Reduce Boating Deaths

Title: Mandatory Life Jacket Laws Could Reduce Boating Deaths
Category: Health News
Created: 8/21/2015 12:00:00 AM
Last Editorial Review: 8/24/2015 12:00:00 AM




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Ubisoft is being sued over The Crew in a lawsuit that compares the server shutdown to a bumperless pinball machine

"Imagine you buy a pinball machine, and years later, you enter your den to go play it, only to discover that all the paddles are missing, the pinball and bumpers are gone, and the monitor that proudly displayed your unassailable high score is removed". As reported by Polygon, that's an argument put forth by a new lawsuit against Ubisoft, filed by two Californian players of The Crew. They're suing the company in a proposed class action lawsuit over shutting down the racing game's servers, rendering it unplayable.

Read more




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Current laws cannot protect civilians in space if something goes wrong

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FDA increases enforcement of import laws related to heavy metals, illegal colors and more

The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries. The agency updates and modifies the alerts as needed. Recent modifications to FDA’s import alerts, as posted by the agency, are listed below. Use the chart below to view import alerts.... Continue Reading




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California Adopts a Bundle of AI & Privacy Laws, Most Controversial Bills Vetoed (Updated)

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Brazen Scofflaws? Are Pharma Companies Really Completely Ignoring FDAAA?

Results reporting requirements are pretty clear. Maybe critics should re-check their methods?

Ben Goldacre has rather famously described the clinical trial reporting requirements in the Food and Drug Administration Amendments Act of 2007 as a “fake fix” that was being thoroughly “ignored” by the pharmaceutical industry.

Pharma: breaking the law in broad daylight?
He makes this sweeping, unconditional proclamation about the industry and its regulators on the basis of  a single study in the BMJ, blithely ignoring the fact that a) the authors of the study admitted that they could not adequately determine the number of studies that were meeting FDAAA requirements and b) a subsequent FDA review that identified only 15 trials potentially out of compliance, out of a pool of thousands.


Despite the fact that the FDA, which has access to more data, says that only a tiny fraction of studies are potentially noncompliant, Goldacre's frequently repeated claims that the law is being ignored seems to have caught on in the general run of journalistic and academic discussions about FDAAA.

And now there appears to be additional support for the idea that a large percentage of studies are noncompliant with FDAAA results reporting requirements, in the form of a new study in the Journal of Clinical Oncology: "Public Availability of Results of Trials Assessing Cancer Drugs in the United States" by Thi-Anh-Hoa Nguyen, et al.. In it, the authors report even lower levels of FDAAA compliance – a mere 20% of randomized clinical trials met requirements of posting results on clinicaltrials.gov within one year.

Unsurprisingly, the JCO results were immediately picked up and circulated uncritically by the usual suspects.

I have to admit not knowing much about pure academic and cooperative group trial operations, but I do know a lot about industry-run trials – simply put, I find the data as presented in the JCO study impossible to believe. Everyone I work with in pharma trials is painfully aware of the regulatory environment they work in. FDAAA compliance is a given, a no-brainer: large internal legal and compliance teams are everywhere, ensuring that the letter of the law is followed in clinical trial conduct. If anything, pharma sponsors are twitchily over-compliant with these kinds of regulations (for example, most still adhere to 100% verification of source documentation – sending monitors to physically examine every single record of every single enrolled patient - even after the FDA explicitly told them they didn't have to).

I realize that’s anecdotal evidence, but when such behavior is so pervasive, it’s difficult to buy into data that says it’s not happening at all. The idea that all pharmaceutical companies are ignoring a highly visible law that’s been on the books for 6 years is extraordinary. Are they really so brazenly breaking the rules? And is FDA abetting them by disseminating incorrect information?

Those are extraordinary claims, and would seem to require extraordinary evidence. The BMJ study had clear limitations that make its implications entirely unclear. Is the JCO article any better?

Some Issues


In fact, there appear to be at least two major issues that may have seriously compromised the JCO findings:

1. Studies that were certified as being eligible for delayed reporting requirements, but do not have their certification date listed.

The study authors make what I believe to be a completely unwarranted assumption:

In trials for approval of new drugs or approval for a new indication, a certification [permitting delayed results reporting] should be posted within 1 year and should be publicly available.

It’s unclear to me why the authors think the certifications “should be” publicly available. In re-reading FDAAA section 801, I don’t see any reference to that being a requirement. I suppose I could have missed it, but the authors provide a citation to a page that clearly does not list any such requirement.

But their methodology assumes that all trials that have a certification will have it posted:

If no results were posted at ClinicalTrials.gov, we determined whether the responsible party submitted a certification. In this case, we recorded the date of submission of the certification to ClinicalTrials.gov.

If a sponsor gets approval from FDA to delay reporting (as is routine for all drugs that are either not approved for any indication, or being studied for a new indication – i.e., the overwhelming majority of pharma drug trials), but doesn't post that approval on the registry, the JCO authors deem that trial “noncompliant”. This is not warranted: the company may have simply chosen not to post the certification despite being entirely FDAAA compliant.

2. Studies that were previously certified for delayed reporting and subsequently reported results

It is hard to tell how the authors treated this rather-substantial category of trials. If a trial was certified for delayed results reporting, but then subsequently published results, the certification date becomes difficult to find. Indeed, it appears in the case where there were results, the authors simply looked at the time from study completion to results posting. In effect, this would re-classify almost every single one of these trials from compliant to non-compliant. Consider this example trial:


  • Phase 3 trial completes January 2010
  • Certification of delayed results obtained December 2010 (compliant)
  • FDA approval June 2013
  • Results posted July 2013 (compliant)


In looking at the JCO paper's methods section, it really appears that this trial would be classified as reporting results 3.5 years after completion, and therefore be considered noncompliant with FDAAA. In fact, this trial is entirely kosher, and would be extremely typical for many phase 2 and 3 trials in industry.

Time for Some Data Transparency


The above two concerns may, in fact, be non-issues. They certainly appear to be implied in the JCO paper, but the wording isn't terribly detailed and could easily be giving me the wrong impression.

However, if either or both of these issues are real, they may affect the vast majority of "noncompliant" trials in this study. Given the fact that most clinical trials are either looking at new drugs, or looking at new indications for new drugs, these two issues may entirely explain the gap between the JCO study and the unequivocal FDA statements that contradict it.

I hope that, given the importance of transparency in research, the authors will be willing to post their data set publicly so that others can review their assumptions and independently verify their conclusions. It would be more than a bit ironic otherwise.

[Image credit: Shamless lawlessness via Flikr user willytronics.]


Thi-Anh-Hoa Nguyen, Agnes Dechartres, Soraya Belgherbi, and Philippe Ravaud (2013). Public Availability of Results of Trials Assessing Cancer Drugs in the United States JOURNAL OF CLINICAL ONCOLOGY DOI: 10.1200/JCO.2012.46.9577




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CA Intermediate Corporate and Other Laws Question Paper New Course September 2024

Download CA Inter Corporate and Other Laws New Course Question Papers Sep 2024 in PDF. For other question papers of CA IPC May 2023, Nov 2023, May 2023, Nov 2022, May 2022, Dec 2021, July 2021, Nov 2020, Nov 2019, May 2019, Nov 18, May 18, Nov 2017, May 17, Nov 2016, may 2016, CA IPC Nov 2015, CA IPC may 2015, CA IPC Nov 2014 check similar section. Previous years business law, Ethics and Communication CA Inter IPC question papers can also be downloaded using Search. You can also search and download may 2015 Final question papers here. We are providing ca final question papers of may 2016 for Financial Reporting FR, Advanced Financial Management AFM, Advanced Auditing and Professional Ethics, Corporate & Allied business laws, Advanced & Management Accounting AMA, Information Systems Control & Audit ISCA, Direct Tax business laws DT, Indirect Tax business laws IDT and Inter/IPC may 2015 question papers for Advanced Accounting, Taxation, Advanced Accounting , Auditing & Assurance, Information Technology & Strategic Management ITSM