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LG Display’s 27-inch DFR Gaming OLED panel wins SID’s ‘Display of the Year’

SEOUL, South Korea, April 29, 2026 /PRNewswire/ — LG Display, the world’s leading innovator of display technologies, announced that its 27-inch 540/720Hz Dynamic Frequency & Resolution (DFR) Gaming OLED panel has been awarded “Display of the Year” by the Society for Information Display (SID), receiving high acclaim for redefining the gaming display paradigm and accelerating market differentiation.

LG Display’s 27-inch DFR Gaming OLED panel wins SID’s ‘Display of the Year’
LG Display’s 27-inch DFR Gaming OLED panel wins SID’s ‘Display of the Year’

The “Display of the Year” award is SID’s most prestigious distinction, presented to the most groundbreaking display product launched during the previous year that is expected to lead the future of the industry.

This achievement recognizes LG Display’s new user-centered display paradigm. The product’s standout feature is the company’s proprietary DFR technology, which allows users to freely select the mode that suits their preferred gaming style.

High-refresh-rate mode particularly proves its value in game genres where rapid screen transitions are essential and victory is decided in a split second — like first-person shooters or racing games. By supporting an industry-leading refresh rate of 720Hz with HD resolution, this mode eliminates ghosting and motion blur even in the fastest scenes, enabling overwhelming gaming performance.

High-resolution mode provides an optimized visual experience for games based on stunning graphics. It simultaneously delivers QHD resolution and a 540Hz refresh rate. To overcome the conventional limitation where picture quality drops once the refresh rate exceeds 500Hz, LG Display applied a proprietary algorithm, securing the two core elements of a high refresh rate and high picture quality.

As a result, the panel obtained ClearMR 21000 certification, the highest rating from the Video Electronics Standards Association (VESA).

“Our goal is to continue leading the gaming display market by leveraging LG Display’s differentiated OLED technologies and relentless pursuit of innovation,” said Young-seok Choi, Chief Technology Officer of LG Display.

SID is the world’s largest display society with more than 7,000 industry experts, researchers, and professors. It hosts Display Week annually, featuring new technologies, product exhibitions, and academic presentations. SID Display Week 2026 will take place in Los Angeles, California from May 3 to 8.

※ LG Display 27-inch 540/720Hz (DFR) OLED Gaming Monitor Panel Specifications

Category

High-refresh-rate mode

High-resolution mode

Peak Brightness

1,500nits

1,500nits

Refresh Rate / Resolution

720Hz / HD

540Hz / QHD

Response Time

0.02ms

0.02ms

 

About LG Display
LG Display Co., Ltd. [NYSE: LPL, KRX: 034220] is the world’s leading innovator of display technologies, including thin-film transistor liquid crystal and OLED displays. The company manufactures display panels in a broad range of sizes and specifications primarily for use in TVs, notebook computers, desktop monitors, automobiles, and various other applications, including tablets and mobile devices. LG Display currently operates manufacturing facilities in Korea and China, and back-end assembly facilities in Korea, China, and Vietnam. The company has approximately 70,707 employees operating worldwide. For more news and information about LG Display, please visit www.lgdisplay.com.

Media Contact:
Joo Yeon Jennifer Ha, Team Leader, Communication Team
Email: hjy05@lgdisplay.com

Jyong Biotech Updates Market Access Strategy for Innovative Botanical Drugs, Establishing Multiple Competitive Advantages for New Drug Portfolio

TAIPEI, April 29, 2026 /PRNewswire/ — Jyong Biotech Ltd. (Nasdaq: MENS) (the “Company” or “Jyong Biotech”), a science-driven biotechnology company dedicated to the development and commercialization of innovative plant-derived therapeutics, today announced that it has advanced the market access strategies for its innovative plant-based drugs Botreso® and PCP, after an analysis of their clinical efficacy and competitive advantages.

As previously announced, its first core product, Botreso®, has completed four Phase III clinical trials (API-1) in the United States and Taiwan while its second core product, PCP, has successfully completed its Phase II clinical trial. Overall clinical data indicates that Jyong Biotech’s innovative botanical drugs demonstrate significant differentiated advantages over currently prescribed synthetic chemical drugs.

Safety Profile for Long-Term Use

For middle-aged and elderly men requiring long-term medication, safety is one of the most decisive factor. During the clinical trials – a one-year medication period for Botreso® (Phase III) and a two-year period for PCP (Phase II) – no drug-related serious adverse events were observed, indicating excellent safety and tolerability.

In contrast, current synthetic chemical drugs for BPH treatment are frequently accompanied by side effects such as orthostatic hypotension, erectile dysfunction, and decreased libido. Regulatory and research institutions have associated some synthetic alternatives with serious risks, prompting the US FDA to issue safety announcements regarding high-grade prostate cancer and depression in 2011, and to add suicidal ideation to adverse reaction lists in 2022, alongside independent research linking them to cardiac failure in 2021.

Addressing the Risk of High-Grade Prostate Cancer

Large-scale international clinical trials have shown that while some synthetic drugs for BPH treatment reduce overall prostate cancer incidence, they may paradoxically increase the proportion of high-grade prostate cancer (Gleason Score ≥ 7) when cancer does occur, raising significant clinical safety concerns.

The PCP Phase II trial was a rare large-scale, long-term study in Taiwan, conducted across 20 major hospitals. It involved 135 urologists (representing more than one-tenth of the profession in Taiwan) and 702 subjects over a two-year period. It represents one of the world’s first clinical trials of a botanical new drug conducted in Taiwan specifically for prostate cancer prevention. Results indicated that PCP shows a trend in reducing both overall prostate cancer incidence and the risk of high-grade prostate cancer, effectively addressing medical community concerns regarding the risks of current therapies.

Comprehensive “Treatment + Prevention + Metabolic Management”

Based on clinical data from the clinical trials conducted by the Company, the Company believes that it is establishing a differentiated product positioning:

  • Improves Lower Urinary Tract Symptoms (LUTS): Effectively addresses symptoms associated with enlarged prostates.
  • Prostate Cancer Prevention: Demonstrates preventative clinical potential.
  • Metabolic and Cardiovascular Protection: Reduces triglycerides (P=0.05), significantly lowers total cholesterol and LDL (bad cholesterol) (P<0.05) , significantly increases HDL (good cholesterol) (P<0.05) , and maintains stable blood sugar.

This integrated approach provides benefits without negatively affecting blood pressure, liver function, or kidney function. The Company believes that such a comprehensive profile – combining treatment, prevention, and metabolic management – is highly uncommon among current prostate medications and holds strong appeal for men over the age of 40.

Technological Barriers and Competitive Advantages

Due to the inherent complexity and diversity of their compositions, quality control for botanical new drugs is significantly more challenging than for small-molecule chemical drugs. Jianyong Biotech believes it has successfully established a comprehensive technological platform that includes:

  • The purification and establishment of reference standards.
  • The development and validation of analytical methods.
  • The execution of validation analyses and verification processes.

The Company believes this integrated capability creates a high barrier to entry, rendering the products highly difficult to replicate. Furthermore, it effectively mitigates the risks associated with counterfeiting and generic drug competition, which ultimately helps to extend the period of market exclusivity.

Upgraded Market Positioning and Strategic Value

As a Botanical New Drug protected by global patents, Jyong Biotech believes its market strategies leverage several key advantages:

  • Pricing Power: The unique metabolic protection and safety profile allow for premium pricing over off-patent generics, making it attractive to out-of-pocket and high-end medical markets.
  • Licensing Potential: The combination of high tolerability, excellent safety (no severe adverse reactions), and multiple clinical benefits makes it an ideal target for international pharmaceutical partnerships.
  • Market Scalability: Extends the product scope from a treatment-oriented approach into the fields of preventative medicine and health management.

Globally, over 500 million men aged 50 and above seek treatment for Benign Prostatic Hyperplasia (BPH). The global BPH drug market, valued at $4.1 billion in 2020, is projected to reach $9.8 billion by 2026. While the current treatment market generates approximately $6.5 to $7 billion annually, this figure reflects price reductions due to patent expirations; if valued at on-patent pricing, this market potential exceeds $20 billion annually*.

“Due to their complex composition, botanical new drugs present significant quality control challenges compared to small-molecule chemical drugs,” stated Fu-Feng Kuo, Chairwoman and CEO of Jyong Biotech. “We have established a robust technology platform encompassing the purification of standard references, the development and validation of analytical methods, and the execution of validation analysis. This high barrier to entry makes imitation difficult, mitigates generic competition, and helps extend the period of market exclusivity.”

“Botreso® is the first orally administered botanical new drug developed in Taiwan to receive US FDA Phase III clinical trial (API-1) IND approval and complete four Phase III trials,” Kuo said. “Holding multi-national invention patents across Asia, the Americas, and the EU, Jyong Biotech has signed letters of intent and investment plans with several international pharmaceutical companies. The company aims to continue expanding strategic, royalty-bearing partnerships to support its global market expansion.”

As of present day, Botreso® and PCP remain investigational new drug candidates and have not been approved for commercial use in any jurisdiction. Jyong Biotech will comply with applicable regulatory disclosure obligations and provide timely, accurate, and complete updates on material developments.

*Data source: BMC Urology 2025 (Global Epidemiology); IMARC BPH market report; P&S Intelligence market data; Global Market Statistics; Grand View Research (device market); Market Analytics (drug segmentation).

About Jyong Biotech Ltd.

Headquartered in Taiwan, Jyong Biotech Ltd. is a science-driven biotechnology company committed to developing and commercializing innovative and differentiated new drugs (plant-derived), mainly specializing in the treatment of urinary system diseases, with an initial focus on the markets of the U.S., the EU and Asia. Since its inception in 2002, the Company has built integrated capabilities that encompass all key functionalities of drug development, including early-stage drug discovery and development, pharmacology, toxicology, clinical trials, regulatory affairs, manufacturing, and commercialization. Leveraging strong research and development capabilities and a proprietary platform, the Company has been developing a series of botanical drug candidates, including its primary botanical drug candidate, BOTRESO®, another clinical-stage botanical drug candidate, and other preclinical-stage botanical drug candidates. The Company endeavors to develop and supply first-class innovative drugs to meet customers’ health needs and seeks to be a valuable business organization that is held in high esteem by the public.

For more information, please visit: https://www.jyongbio.com/, https://jyongir.com/.

Forward-Looking Statement

This press release contains forward-looking statements. Forward-looking statements include statements concerning plans, objectives, goals, strategies, future events or performance, and underlying assumptions and other statements that are other than statements of historical facts. When the Company uses words such as “may, “will, “intend,” “should,” “believe,” “expect,” “anticipate,” “project,” “estimate” or similar expressions that do not relate solely to historical matters, it is making forward-looking statements. Forward-looking statements are not guarantees of future performance and involve risks and uncertainties that may cause the actual results to differ materially from the Company’s expectations discussed in the forward-looking statements. These statements are subject to uncertainties and risks including, but not limited to, the uncertainties related to market conditions and other factors discussed in the “Risk Factors” section of the registration statement, prospectuses, annual and interim reports, and other filings with the SEC. For these reasons, among others, investors are cautioned not to place undue reliance upon any forward-looking statements in this press release. Additional factors are discussed in the Company’s filings with the SEC, which are available for review at www.sec.gov. The Company undertakes no obligation to publicly revise these forward-looking statements to reflect events or circumstances that arise after the date hereof.

For more information, please contact:
Jyong Biotech Ltd.
ir@jyongbio.com

Investor Relations
WFS Investor Relations Inc.
Email: services@wfsir.com
Phone: +1 628 283 9214

Global Times: From seawater to green hydrogen, and beyond, Qingdao charts a new growth path

BEIJING, April 29, 2026 /PRNewswire/ — On a clear day at the sprawling coastal industrial park of Sinopec Qingdao Refining & Chemical Co, a major oil refiner in the country, a modest but groundbreaking facility hums quietly by the shore.

Against the backdrop of a massive industrial complex that stretches for several kilometers stands a shipping-container-sized assembly of pipes and meters arranged in a maze-like structure – the heart of China’s first 100-kilowatt factory-scale seawater-to-hydrogen direct electrolysis project, which is turning seawater and sunshine into green fuel.

“After more than a year of research and development, the project has completed over 1,000 hours of cumulative operation and is ready to scale up from research to mass production of green hydrogen,” Qin Weilong, a process expert at Sinopec Qingdao Refining & Chemical and technical director of the “Oriental Hydrogen Island” project, told the Global Times.

Unlike conventional industrial hydrogen production, which often relies on purified freshwater or fossil fuels, this project uses pre‑treated seawater directly, powered entirely by renewable electricity generated from offshore solar photovoltaic panels at a nearby solar farm.

In 2025, China’s total marine economy output reached nearly 11.02 trillion yuan ($1.62 trillion), with a year-on-year growth of 5.5 percent, and accounting for 7.9 percent of the country’s GDP. Utilizing its inherent resources and technological innovation, Qingdao is a prime example of China’s efforts to promote the high-quality development of the marine economy.

Green energy from the blue ocean

The “Oriental Hydrogen Island” produces 20 cubic meters of green hydrogen per hour. The electricity comes from 13 megawatts of installed offshore solar capacity – enough that one hour of sunlight can generate roughly 2,600 standard cubic meters of green hydrogen. By consuming renewable power on site, the project dramatically cuts electricity costs for hydrogen production.

Pointing to a container-sized device covered with pipes and meters, Qin said, “This is our photovoltaic green power plus seawater hydrogen production unit.”

The term “green hydrogen” refers to hydrogen produced with near-zero carbon emissions, typically via electrolysis of water using renewable energy. This distinguishes it from “gray hydrogen” that comes from fossil fuels and “blue hydrogen” that is extracted from industrial byproducts, making it dependent on petrochemical processes. The Oriental Hydrogen Island project represents a clean break: all its input energy comes from solar.

“These solar panels produce enough green electricity in one hour to make about 2,600 standard cubic meters of green hydrogen,” Qin said, pointing to the offshore array. “Direct seawater electrolysis saves both freshwater and the high cost of desalination. It’s a game-changer.”

This on-site trial has fully demonstrated the technical feasibility of using intermittent renewable power for green hydrogen production, opening a new path for large-scale consumption of renewable electricity in the future, Qin said.

Yet Qin remains measured about the journey ahead. “We have validated the feasibility of directly obtaining hydrogen from seawater,” he said. “The ocean offers an endless source of raw materials and power for green hydrogen. We are full of confidence for the future.”

Less than two kilometers away stands China’s first carbon-neutral hydrogen refueling station, which sources its green hydrogen from the “Oriental Hydrogen Island.”

A special hydrogen tanker from Shandong-based Sino Hydrogen Co, a hydrogen supply solutions provider, slowly entered the station. “Refueling 35 kilograms of hydrogen takes only 15 minutes,” said Gao Gang, a station worker. The tankers deliver green hydrogen to downstream users. “We also refuel some of Qingdao’s hydrogen fuel‑cell buses – that process takes about eight minutes and provides enough energy for a full day of operation.”

Experts note that fast refueling and zero emissions, as only water vapor is released when power is generated, are key advantages of hydrogen energy. When applied to urban transportation, hydrogen fuel cell vehicles can add significant “greenness” to the city’s mobility transition.

The outline of China’s 15th Five-Year Plan (2026-30), recently released, calls for focusing on key areas that will drive future development, building a full-chain cultivation system for future industries, and promoting hydrogen energy and nuclear fusion as new economic growth points.

Shandong Province, a major energy and chemical hub, stands to benefit greatly from this technology. A Sinopec Qingdao manager said that seawater-based hydrogen production can support deep decarbonization efforts at coastal steel and petrochemical sectors, enable zero-carbon scenarios for hydrogen-powered heavy trucks, ocean-going vessels, and island energy supply, and help create zero-carbon industrial clusters.

An innovation park that hears the sea’s call

Qingdao, China’s second-largest foreign trade port, is not only harnessing the sea for clean energy but also leveraging its coastal location to attract global talent, technology, and investment. Just a short drive from the port, in the city’s West Coast New Area, lies an elegant business park set against a backdrop of hills and water. On a black marble pedestal by a waterfront terrace, some 30 national flags flutter in the breeze – a visible sign of the park’s international character. This is the Sino-German Ecopark.

Amid the greenery and birdsong, the rumble of container trucks can be heard if sea winds blow from the direction of the nearby Qingdao Port. “Proximity to the port is a top consideration for our tenants,” Kerstin Kaehler, branch manager of the German Enterprise Centre Qingdao, told the Global Times. Kaehler, who is in her early 50s, has spent 27 years in China fostering business communication and helping German and other foreign companies successfully establish themselves in the country.

The center currently houses 44 tenants, most of them small and medium-sized enterprises (SMEs). Half are Chinese companies; the other half come from Germany, the US, Japan, the UK, Singapore, and other nations. “At the end of 2019, we had 27 tenants. Now we have 44,” Kaehler said.

Despite changing market dynamics, she noted that foreign companies’ interest in the Chinese market has not waned. Notably, demand for co-working spaces or small offices is strong, a trend she expects to continue.

“If a company is a world market leader, it is usually also innovative. If they are, then they are willing and able to learn and draw inspiration from everything happening in China in that field,” Kaehler said. “Especially now, as China is rolling out its new five-year economic plan, I believe that foreign companies – especially German SMEs – have a big role to play in China’s efforts to build a modern industrial system.”

From extracting green hydrogen from the sea to attracting foreign expertise and investing in coastal health and wellness resources, Qingdao is steadily implementing the central government’s strategy to advance Chinese modernization by efficiently utilizing marine resources, promoting the high-quality development of the marine economy, and forging a Chinese path of leveraging marine resources to achieve strength.

Alma Unveils Longevity Approach at Alma Academy, Advancing Long-Term Skin Performance

CAESAREA, Israel, April 29, 2026 /PRNewswire/ — Alma, a Sisram Medical company and a global leader in medical aesthetic solutions, unveiled its longevity strategy at its global Alma Academy, outlining its shift toward a continuous care model and a new long-term growth approach.

A shift to a continuous care model and a long-term growth strategy: Eyal Ben David, CEO of Alma, introduces the company’s new approach to longevity
A shift to a continuous care model and a long-term growth strategy: Eyal Ben David, CEO of Alma, introduces the company’s new approach to longevity

In remarks to 430 physicians from 45 countries, Alma CEO Eyal Ben David outlined the company’s transition toward a platform enabling continuous, outcomes-driven care.

“Longevity is redefining aesthetics as a discipline of performance over time,” said Mr. Ben David. “The focus is on enhancing how skin functions, adapts, and maintains quality, through controlled biological responses that drive regeneration, resilience, and structural improvement. This approach enables practitioners to deliver measurable, sustained outcomes and build long-term value through consistent skin performance. At the core of this is the operating system of modern aesthetics, an integrated, end-to-end system designed to orchestrate the entire patient journey and redefine how care is delivered over time.”

The company highlighted that this approach reflects a broader shift in consumer expectations, with patients increasingly prioritizing prevention, long-term results, and personalized experiences. Alma’s longevity approach focuses on enhancing skin function and quality over time, starting earlier, extending engagement, and delivering sustained, measurable outcomes through an integrated ecosystem of technologies designed to activate the skin’s natural regenerative and adaptive responses.

This year’s global summit brought together 19 world-class experts from across the industry to share insights, research, and real-world case studies. Notable speakers included Dr. Spero Theodorou, Prof. Ofir Artzi, Dr. Pablo Naranjo, Dr. Tino Solomon, and Dr. Jaerim Kim, alongside other leading experts from around the world.

Sessions covered key clinical indications shaping the future of medical aesthetics, including skin rejuvenation, vascular indications, acne and acne scars, pigmentation, skin laxity, scars, and the treatment of challenging skin conditions, reflecting the industry’s growing emphasis on comprehensive, long-term patient care.

Alma Academy continues to serve as a premier global platform for education, innovation, and collaboration, bringing together leading practitioners to exchange knowledge, advance clinical excellence, and experience the latest technologies through live demonstrations.

About Alma

Alma is a global leader in medical aesthetic solutions, with over 25 years of innovation. The company empowers practitioners to deliver safe, effective, and transformative treatments through state-of-the-art, clinically proven solutions spanning energy-based lasers, skin analysis, injectables, and advanced skincare. Alma’s multiple award-winning products have set new benchmarks in the medical aesthetics industry, combining clinical excellence with groundbreaking innovation.

Media Inquiries

prglobal@almalasers.com

 

Continue to serve as a premier global platform for aesthetic innovation and education: Alma Academy
Continue to serve as a premier global platform for aesthetic innovation and education: Alma Academy

 

 

Alma Unveils Longevity Approach at Alma Academy, Advancing Long-Term Skin Performance

CAESAREA, Israel, April 29, 2026 /PRNewswire/ — Alma, a Sisram Medical company and a global leader in medical aesthetic solutions, unveiled its longevity strategy at its global Alma Academy, outlining its shift toward a continuous care model and a new long-term growth approach.

A shift to a continuous care model and a long-term growth strategy: Eyal Ben David, CEO of Alma, introduces the company’s new approach to longevity
A shift to a continuous care model and a long-term growth strategy: Eyal Ben David, CEO of Alma, introduces the company’s new approach to longevity

In remarks to 430 physicians from 45 countries, Alma CEO Eyal Ben David outlined the company’s transition toward a platform enabling continuous, outcomes-driven care.

“Longevity is redefining aesthetics as a discipline of performance over time,” said Mr. Ben David. “The focus is on enhancing how skin functions, adapts, and maintains quality, through controlled biological responses that drive regeneration, resilience, and structural improvement. This approach enables practitioners to deliver measurable, sustained outcomes and build long-term value through consistent skin performance. At the core of this is the operating system of modern aesthetics, an integrated, end-to-end system designed to orchestrate the entire patient journey and redefine how care is delivered over time.”

The company highlighted that this approach reflects a broader shift in consumer expectations, with patients increasingly prioritizing prevention, long-term results, and personalized experiences. Alma’s longevity approach focuses on enhancing skin function and quality over time, starting earlier, extending engagement, and delivering sustained, measurable outcomes through an integrated ecosystem of technologies designed to activate the skin’s natural regenerative and adaptive responses.

This year’s global summit brought together 19 world-class experts from across the industry to share insights, research, and real-world case studies. Notable speakers included Dr. Spero Theodorou, Prof. Ofir Artzi, Dr. Pablo Naranjo, Dr. Tino Solomon, and Dr. Jaerim Kim, alongside other leading experts from around the world.

Sessions covered key clinical indications shaping the future of medical aesthetics, including skin rejuvenation, vascular indications, acne and acne scars, pigmentation, skin laxity, scars, and the treatment of challenging skin conditions, reflecting the industry’s growing emphasis on comprehensive, long-term patient care.

Alma Academy continues to serve as a premier global platform for education, innovation, and collaboration, bringing together leading practitioners to exchange knowledge, advance clinical excellence, and experience the latest technologies through live demonstrations.

About Alma

Alma is a global leader in medical aesthetic solutions, with over 25 years of innovation. The company empowers practitioners to deliver safe, effective, and transformative treatments through state-of-the-art, clinically proven solutions spanning energy-based lasers, skin analysis, injectables, and advanced skincare. Alma’s multiple award-winning products have set new benchmarks in the medical aesthetics industry, combining clinical excellence with groundbreaking innovation.

Media Inquiries

prglobal@almalasers.com

Photo – https://laotiantimes.com/wp-content/uploads/2026/04/alma_1-1.jpg
Photo – https://laotiantimes.com/wp-content/uploads/2026/04/alma_2-1.jpg
Logo – https://laotiantimes.com/wp-content/uploads/2026/04/alma_logo-1.jpg

Continue to serve as a premier global platform for aesthetic innovation and education: Alma Academy
Continue to serve as a premier global platform for aesthetic innovation and education: Alma Academy

 

 

TestMu AI Launches Kane CLI, the New Browser Automation Tool Built for AI Agents and Developers

The terminal-native browser verification tool ships today with native support for Claude Code, Codex CLI, Cursor, and Gemini CLI, and it’s free to start

SAN FRANCISCO and NOIDA, India, April 29, 2026 /PRNewswire/ — TestMu AI (formerly LambdaTest), the world’s first full-stack Agentic Quality Engineering platform, today announced the launch of Kane CLI, a new browser automation tool that runs directly from the terminal. Kane CLI is the first tool designed simultaneously for human developers and AI coding agents, closing the gap between code generation and verified browser execution.

AI coding agents have transformed how software gets written, as AI agents are shipping code faster than any QA team can click through flows manually. Features ship from prompts. Bugs get fixed in seconds. But the development loop has never fully closed: no agent can open a browser and verify that what it built actually works. That step still falls to a human. Kane CLI is built to close this loop.

Teams build features, spot bugs, ship code, and run agents. Kane CLI is the verification layer for all of it. Developers and QA engineers describe the flow and get pass or fail with a full step trace and screenshot before the PR goes up. Designers and PMs verify fixes and broken flows without filing a ticket or waiting for a developer, then drop the shareable evidence link straight into Slack or Jira.

AI agents like Claude Code, Codex CLI, Cursor, and Gemini CLI build a feature; Kane CLI is the missing tool that tells them whether it actually works in the local Chrome browser.

Key Capabilities of Kane CLI include:

  • Intent-based browser control: Operates purely on intent, requiring no selectors or underlying code.
  • Resilient runs: Kane CLI does not return halfway. It adapts and pushes through, up to 50 steps per flow, until the full journey is verified. Other tools break on the first change. Kane CLI finishes the run.
  • Playwright export: Converts plain English test flows into native Playwright test code with one command.
  • Automated bug discovery: Actively monitors and surfaces unexpected behaviors while the test flow is running.
  • Vision-based dynamic waiting: Detects loaders and animations on screen before acting. Not network-based. Handles canvas, Shadow DOM, and element frameworks that cannot be resolved.
  • Ask the tool for OTPs and CAPTCHAs: When an automated flow hits an OTP screen or a CAPTCHA, it does not fail silently. Kane CLI pauses, asks the human to handle that one step, and then continues the run. For AI agents, this is human-in-the-loop without stopping the entire workflow.
  • Two-way script migration: Convert existing Playwright or Selenium scripts to Kane CLI. Convert Kane CLI tests back to Playwright. No rewrite from scratch.
  • Inbuilt Test Manager sync: Every test case created locally is also saved remotely. Shareable proof attached automatically.
  • CI/CD ready: Runs headlessly in GitHub Actions, GitLab CI, Jenkins, and Bitbucket Pipelines. Standard exit codes plug into pipeline control flow without any custom scripting.
  • Contextual authoring: Give Kane CLI context about your app, and it authors parallel test cases across multiple browser sessions from a single prompt.

Three Ways to Run

Kane CLI ships with three modes so humans and agents can consume it the same way from the same terminal.

  • Interactive TUI – No arguments needed. A full terminal UI opens for exploring, iterating, and chaining tests across a live browser session.
  • Headless CLI – Add –headless for scriptable, display-free runs. Built for shell scripts and CI pipelines.
  • Agent Mode – Add –agent –headless. Outputs structured NDJSON that Claude Code, Codex CLI, and Gemini CLI read natively to decide what to do next.

Asad Khan, CEO & Co-Founder, TestMu AI, said, “For years, the bottleneck in software was writing the code. Vibe coding removed that. Teams are shipping more software, faster, than at any point in the history of our industry. But it exposed a new bottleneck most teams haven’t named yet: trust. Every feature that ships from a prompt is a feature nobody has actually verified. At agentic speed, ‘a human will click through it later’ is not a plan — it’s a liability, compounding at the speed of AI. It’s a growing pile of unverified work. That’s why we built Kane CLI. One terminal command, a real browser, pass or fail. Software has always trusted the people who wrote it. Now, for the first time, it has to trust the machines. Kane CLI is how trust scales in the agentic era.”

As part of its launch, TestMu AI is offering bonus credits for the first three months to teams that activate a paid plan during the introductory period. The offer is designed to give engineering and quality teams full access to Kane CLI’s cloud capabilities.

Kane CLI is available today, free to start. Install via npm or brew, log in, and run your first flow.

Installation command for Kane CLI via npm – npm install -g @testmuai/kane-cli

Installation command for Kane CLI via Homebrew – brew install LambdaTest/kane/kane-cli

Or building with an AI agent? Point it to testmuai.com/kane-cli/agents.md

For a quick start, visit the docs at testmuai.com/support/docs/kane-cli-introduction/ and to learn more, visit testmuai.com/kane-cli

About TestMu AI (Formerly LambdaTest)

TestMu AI is the world’s first Agentic AI-powered Quality Engineering platform, designed to enable organizations to automate and scale testing with intelligence at its core. By combining autonomous capabilities with seamless integration across modern development workflows, TestMu AI empowers teams to deliver faster, more reliable, and secure software in an AI-first world.

For more information, visit https://www.testmuai.com/

 

Hong Kong Patient Overcomes Four IVF Failures with Taiwan NUWA Healthcare’s Precision Medicine; Taiwan Emerges as Leading Fertility Hub with One-Third the Cost of US and HK

TAIPEI and TAICHUNG, April 29, 2026 /PRNewswire/ — A 38-year-old Hong Kong woman has successfully achieved pregnancy and “graduated” from her fertility journey after four previous failed IVF attempts in Hong Kong. The breakthrough came under the care of Dr. Cheng-Hsuan Wu, Vice Director of NUWA Fertility Center in Taichung, whose medical intervention identified a long-overlooked case of chronic endometritis and utilized advanced PGT-A and ERA screening technologies to ensure a successful embryo transfer.

Chronic Endometritis: The Hidden Culprit Behind Recurrent Implantation Failure

Upon her initial arrival at the clinic, the patient was disheartened, believing this was her final opportunity. Following a thorough hysteroscopy, Dr. Wu identified Chronic Endometritis as the critical cause of her past failures. Dr. Wu explained that chronic inflammation of the uterine lining alters the micro-environment, making it difficult for embryos to implant—a hidden factor frequently overlooked in cases of recurrent implantation failure.

Dr. Wu further noted that according to medical literature, approximately 30% of habitual miscarriages and recurrent failures are caused by chronic endometritis. For this patient, a two-week course of antibiotic treatment was administered to resolve the inflammation before officially commencing the IVF cycle.

Cutting-Edge Technology: PGT-A and ERA Identify the “Golden Window” for Implantation

To maximize the success rate of a single transfer for a patient with multiple previous failures, Dr. Wu utilized two key technologies:

  • PGT-A (Preimplantation Genetic Testing for Aneuploidy): Ideal for advanced maternal age or those with recurrent miscarriages. By screening for embryos with the correct number of chromosomes, PGT-A significantly reduces miscarriage rates and boosts the pregnancy rate per transfer.
  • ERA (Endometrial Receptivity Analysis): Every woman has a unique “window of implantation”. Approximately 30% of women have a window that differs from the standard timing. ERA uses genetic testing to calculate the precise hour for transfer, ensuring the embryo is introduced when the uterine lining is at its most receptive state.

By combining high-quality embryos screened via PGT-A with the precise timing determined by ERA, Dr. Wu carefully transferred a healthy embryo, resulting in an immediate pregnancy for the patient who had nearly given up hope.

Taiwanese Reproductive Medicine: A Top Choice in Asia

Dr. Wu observed a significant increase in patients traveling to Taiwan from Hong Kong, Macau, Japan, Southeast Asia, Europe, and the U.S. for egg freezing, IVF, or donor egg programs. He highlighted three primary reasons for this trend:

  1. Technical Success Rates: Taiwan’s IVF success rate is ranked second in the world, following only the United States. NUWA Healthcare features high-specification laboratories and professional embryologists, supported by precision monitoring systems that ensure treatment stability.
  2. Cost Competitiveness: The cost of IVF and egg freezing in Taiwan is approximately one-third of the prices in the U.S. and Hong Kong, offering world-class medical services at a more accessible price point.
  3. Comprehensive Medical Support: With frequent flights between Hong Kong and Taiwan and multi-language support, NUWA Healthcare offers a seamless experience. The clinic provides online consultations and flexible weekend appointments, significantly reducing the temporal and psychological burden on international patients.

“Witnessing the transformation of a patient’s despair into the joy of pregnancy not only fulfills a family’s dream but also proves the technical prowess and compassionate care of Taiwan’s medical sector on the international stage,” Dr. Wu emphasized.

Dr. Cheng-Hsuan Wu of NUWA Healthcare notes the growing number of Hong Kong patients traveling to Taiwan for egg freezing or IVF treatments reflects Taiwan's advanced medical capabilities.
Dr. Cheng-Hsuan Wu of NUWA Healthcare notes the growing number of Hong Kong patients traveling to Taiwan for egg freezing or IVF treatments reflects Taiwan’s advanced medical capabilities.

For more international success stories from NUWA Healthcare:
https://www.nuwacare.com/zh-TW/stories/intl-Healthcare-Center/1

Information on IVF and Egg Freezing Seminars:
https://www.nuwacare.com/zh-TW/news/seminars/1

Comparison Guide: IVF in Hong Kong vs. Taiwan:
https://www.nuwacare.com/zh-TW/health-education/hongkong-taiwan-ivf-price

Seven Golds for Seven Wines: Spy Valley Named New Zealand Winery of the Year at London Wine Competition

BLENHEIM, New Zealand, April 29, 2026 /PRNewswire/ — Spy Valley Wines has achieved a clean sweep at the London Wine Competition 2026, securing gold medals for all seven wines entered and being named Winery of the Year New Zealand.

The winning line-up included the 2023 Envoy by Spy Valley Sauvignon Blanc, 2024 Spy Valley Chardonnay, and 2025 Spy Valley Sauvignon Blanc, alongside a diverse mix of varietals.

Widely regarded as one of the industry’s most influential competitions, the London Wine Competition is judged by Masters of Wine, Master Sommeliers and senior buyers, assessing wines on quality, value and market appeal.

“To be recognised on this stage is incredible,” said owner and managing director Amanda Johnson. “We’ve always believed that staying true to our land and standards would deliver results. This is a proud moment for our entire team.”

The result builds on recent international success, including Best New Zealand Wine at the 2025 Global Wine & Spirits Awards Asia for its 2024 Gewürztraminer.

Winemaker Emily Gaspard-Clark said the breadth of recognition was particularly rewarding. “Achieving seven golds across multiple varietals shows we’re more than just a Sauvignon Blanc producer.”

Family-owned and operated, Spy Valley Wines has spent more than 30 years developing its estate in Marlborough’s Waihopai Valley, where stony, free-draining soils shape the character and intensity of its wines.

“Achieving consistent excellence across the range means a great deal,” said Head of Viticulture and Winery Operations Adam McCone.

Spy Valley is imported by Broadbent Selections, Richmond, Virginia.

About Spy Valley Wines
Spy Valley Wines is a family-owned estate winery located in New Zealand’s Waihopai Valley, Marlborough. Established in 1993, the winery is known for its expressive Sauvignon Blanc, Pinot Noir, Chardonnay and other aromatics. The estate is a member of Sustainable Winegrowing New Zealand and Appellation Marlborough Wine, and has received multiple international awards, including IWSC New Zealand Wine Producer of the Year.