Dual Miners Changing the Game in Cryptocurrency Mining

DUAL PREMIUM

High Hash Rate

HELSINKI, Finland, April 21, 2022 (GLOBE NEWSWIRE) — Dual Miners has recently earned the distinction becoming the first company ever to introduce an extraordinary range of endothermic cryptocurrency mining rigs. A team of investors working towards making crypto mining simple and profitable. Others have argued that cryptocurrency mining is becoming increasingly difficult, but a new announcement from Dual Miners, which is currently releasing worldwide, the world’s first dual-miner hardware, which uses both SHA-256 and Scrypt to mine.

Visit (https://dualminers.com/products/) for more information. Additionally, the dual-miners can be configured to process transactions for other cryptocurrencies that use the SHA-256 or Scrypt hashing algorithms.

Due to innovative hardware design, Dual Miner’s mining chip, FM9800-XD112, achieves high hash rates while consuming the least amount of energy possible. They come with a built-in controller as well as software already installed. Following an extensive period of testing that included evaluating, prototyping, and extreme-condition pressure testing, the Dual Miner’s DualPro and DualPro Max hardware products, as well as the DualPremium hardware products, are now ready for mass production.

Benefits of Using Dual Miners
What are the advantages of using the Dual Miners Enhance Energy Saver system over other systems? According to the solution’s inventors, each machine will be equipped with a cooling system, a 7-nanometer chip, a noise reduction mechanism, a regulated operational humidity with a power supply, and a wireless network connection (Wi-Fi) or an Ethernet connection. With a short delay, users can mine Bitcoin (BTC), Litecoin (LTC), Monero (XMR), Ethereum (ETH), and several other cryptocurrencies thanks to the algorithm attached to the system, which comprises globally known software and hardware technologies.

Dual Miner’s team consists of seasoned professionals
Dual Miners is a chip design and manufacturing firm with its headquarters in London, United Kingdom. It has a number of teams with in-depth expertise of blockchain technology and technological design.

The company, which has offices on three continents, provides crypto wallet development services as well as graphics processing units to customers. It also has a lot of experience in the fields of Blockchain development and bitcoin mining solutions, among other things.

Due to its extensive experience in the Blockchain business, Dual Miners is a reputable name in the field. It is as a result of this experience that it has been confirmed by firms such as Kraken, ASG Expertise, and FIS International. Dual Miners is putting its previous knowledge to good use once more in order to provide innovative solutions for Cryptocurrency consumers.

Pricing and Availability are important considerations
Dual Miners will cover the delivery fee as well as the customs fee, leaving the consumer to pay only for the unit and receive everything they need to get started without any further charges. “Consumers are now aware that our competitors have been defeated. They are unable to obtain our power or take advantage of our incredibly low electricity expenses. Despite our small size, we have enormous mining power; the DualPremium generates 60 TH/s for Bitcoin and 2.1 GH/s for Litecoin, respectively. It’s the best investment available on the market,” says Michael Scott, Operational Director and Chief Operating Officer of Dual Miners.

About Dual Miners
Founded in 2015, Dual miners, described as the world’s first dual-mining company, was established to develop and sell the world’s first leading dual Cryptocurrency miners using SHA-256 or Scrypt technology. Our goal, starting with the Dual Miners’ DualPro, was to give more power at a lesser cost than was previously available. Dual Miners is headquartered in London, United Kingdom, and has offices all around the world. More information can be found at www.dualminers.com

Michael Scott

PR MANAGER
Michael@dualminers.com
(+358) 41 4001034

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/16dc0570-9425-4920-bce1-4658333d6e81

Anaqua Strengthens AQX IP Management Platform with Automated IDS Solution

New automation tool will drive operational efficiencies, saving time and money, for IP professionals

BOSTON, April 20, 2022 (GLOBE NEWSWIRE) — Anaqua, the leading provider of innovation and intellectual property management technology, today announced plans for the release of its new automated information disclosure solution as part of its AQX IP management offering for corporations and law firms. The new system will help IP professionals save time and money by streamlining and automating the IDS process.

By integrating with USPTO (Private PAIR) and leveraging optical character recognition (OCR) technology on PTO forms (892 and 1449), and international forms and search reports, Anaqua’s IDS system automatically extracts and processes data into an IDS form (SB/08) in just one click. The system also uses external patent data (AcclaimIP), machine learning, and AI tools to automate citation workflow, allowing IP professionals to be in control in managing citations.

“Our clients have shared their deep knowledge of the IDS process and the complicating factors involved in managing the workflow of internal data, external data, government forms, and more,” said Vincent Brault, SVP of Product & Innovation at Anaqua. “By combining commonly known technologies with USPTO and AcclaimIP patent data, we are putting the power of automated IDS management in the hands of our clients.”

“We are committed to delivering capabilities that drive value for our clients in every aspect of the IP management lifecycle and in this case automating the IDS process,” said Bob Romeo, CEO of Anaqua. “Our team is responding to our clients by delivering one of the most efficient and intuitive IDS management systems in the market. We look forward to our customers experiencing increased efficiency and accuracy during their IDS management processes with this release.”

About Anaqua
Anaqua, Inc. is a premium provider of integrated intellectual property (IP) management technology solutions and services for corporations and law firms. Its IP management software solutions, AQX and PATTSY WAVE, both offer best practice workflows with big data analytics and tech-enabled services to create an intelligent environment designed to inform IP strategy, enable IP decision-making, and streamline IP operations, tailored to each segment’s need. Today, nearly half of the top 100 U.S. patent filers and global brands, as well as a growing number of law firms worldwide use Anaqua’s solutions. Over one million IP executives, attorneys, paralegals, administrators, and innovators use the platform for their IP management needs. The company’s global operations are headquartered in Boston, with offices across the U.S., Europe, and Asia. For additional information, please visit anaqua.com, or on LinkedIn.

Company Contact:
Amanda Hollis
Communications Director
Anaqua
617-375-2626
ahollis@Anaqua.com

Concerns Rise Over Sharp Increase in South Africa’s COVID-19 Cases

South Africa has recorded a sharp increase in COVID-19 infections, the highest rate in three months, raising concerns about a possible larger surge in the disease.

South Africa’s National Health Department reported 4,406 new COVID-19 cases in a 24-hour period ending Thursday. The number represents a considerable jump from the 2,846 cases reported the day before, and the previous seven-day average of 1,549.

Adrian Puren, executive director of the National Institute for Communicable Diseases of South Africa, confirmed omicron as the dominant COVID-19 variant in the country and said no new variant of concern has been reported.

He said South Africa is not experiencing a new wave of COVID-19, noting that hospitalizations remain low.

“And as you know, hospitalizations, in other words severe cases, dramatic cases that end up in hospital, either in high care or ICU, I think will be the more appropriate proxy if you like, or indicator, that we have actually reached the fifth resurgence,” Puren said.

When asked how the pandemic is affecting South Africa compared with other countries, he noted that omicron caused high caseloads in Britain and the United States.

“We’re obviously experiencing differences” compared with those countries, “but that’s not to say that our next resurgence won’t resemble that,” Puren said. “And I think that’s the concern — that we need to really be prepared.”

He said even though South Africa plans to do away next month with the National State of Disaster restrictions adopted in the wake of COVID-19, other measures will be put in place. Those have been subject to public comment.

“So I think we’ll probably see a mixture of the things we had in place. So, for example, getting ventilation right. You know, I don’t think people are focused a lot on that. But I think that’s an area, especially for indoor events, offices, restaurants and so forth, that’s absolutely critical,” Puren said.

The main opposition party’s shadow minister for health, Michelle Clarke, said she would be asking parliament’s Health Committee to analyze the rise in numbers when it meets Friday.

“It’s expected during this time to start seeing the resurgence because you’re moving into the colder winter months. People are huddling more,” she said. “So you would see a spread of COVID happening because the environment changes. But if you look at the data that’s been produced within the clusters like, for example, old-age homes, schools, et cetera, it’s definitely not showing that resurgence in those clusters as yet.”

She added that while the party is happy for the sake of the economy that the National State of Disaster restrictions are ending, there had already been 170,000 objections to the new proposed restrictions. Those include unhappiness over the continued 50 percent capacity in venues like restaurants.

Source: Voice of America

WHO ‘Strongly Recommends’ Pfizer’s COVID-19 Pill

The World Health Organization said Friday it “strongly recommended” Pfizer’s COVID-19 antiviral pill Paxlovid for patients with milder forms of the disease who were still at a high risk of hospitalization.

However, the U.N. agency warned it was “extremely concerned” that the inequality in access seen with COVID-19 vaccines would again leave low- and middle-income countries “pushed to the end of the queue.”

U.S. pharma giant Pfizer’s combination of nirmatrelvir and ritonavir was the “superior choice” of treatment for unvaccinated, elderly or immunocompromised people with COVID-19, the WHO’s experts said in the BMJ medical journal.

For the same patients, the WHO also made a “conditional (weak) recommendation” of the antiviral drug remdesivir, made by U.S. biotech firm Gilead, that it had previously recommended against.

The WHO recommended Paxlovid over remdesivir, as well as over Merck’s molnupiravir pill and monoclonal antibodies.

Pfizer’s oral treatment prevents hospitalization more than the “available alternatives, has fewer concerns with respects to harms than molnupiravir, and is easier to administer than intravenous remdesivir and antibodies,” the WHO’s experts said.

The new recommendation was based on the findings of two trials involving almost 3,100 patients which showed that Paxlovid reduced the risk of hospital admission by 85%.

The trials also “suggested no important difference in mortality” and “little or no risk of adverse effects leading to drug discontinuation.”

The recommendation applies to people over the age of 18, but not to pregnant or breastfeeding women.

It also does not apply to patients with a low risk of complications from the disease, because the benefit would be minimal.

The WHO’s experts also declined to give an opinion for patients with severe forms of the disease, due to a lack of data.

The WHO stressed the limitations of such antiviral treatments.

“The medicine can only be administered while the disease is at its early stages,” they said.

This means the patients must quickly test positive and be prescribed the pill by a doctor – all of which can pose obstacles for low- and middle-income countries, the WHO said.

Yet COVID-19 pills have been seen as a potentially huge step in ending the pandemic as they can be taken at home, rather than in hospital.

Patients must start taking their Paxlovid pills within five days of the onset of symptoms – the course then lasts five days.

Remdesivir can be taken within seven days of symptoms setting in, but it is administered intravenously over three days.

The WHO called on Pfizer to “make its pricing and deals more transparent” for Paxlovid.

Lisa Hedman, the WHO’s senior adviser on access to medicines, said that radio station NPR reported a full course of Paxlovid costs $530 in the United States. Another source unconfirmed by WHO gave the price of $250 in an upper-middle-income country.

Remdesivir meanwhile costs $520, Hedman said, but generic versions made by companies in India sell for $53-$64.

There is also a question mark over whether the virus could build resistance to these treatments.

But earlier this month Pfizer CEO Albert Bourla predicted a bright future for treatments like Paxlovid as people grow tired of getting further booster vaccinations.

Coming under fire for prioritizing wealthy countries with its vaccine, Pfizer has agreed to allow some generic drugmakers around the world to make cheaper versions of Paxlovid under a U.N.-backed scheme.

But on Friday the WHO “strongly recommended” that Pfizer let more generic manufacturers produce the drug and “make it available faster at affordable prices.”

Source: Voice of America