Join China Hi-Tech Fair 2024, Where Innovation Meets Global Opportunity

22.7.2024 03:30:00 EEST | Business Wire | Press release

The 26^th China Hi-Tech Fair (CHTF) is set to take place on November 14-16, 2024, at the Shenzhen World Exhibition & Convention Center. As China’s leading and most influential technology event, CHTF offers an unparalleled platform for tech companies worldwide to showcase their latest innovations, engage with industry leaders, and expand their market reach.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20240721948434/en/

Embrace Innovation, Drive Growth

Over the past 25 years, CHTF has established itself as a beacon for technological advancement and international cooperation. With this year’s theme “Technology Leads Development, Industry Integrates Fusion,” the fair underscores the critical role of innovation in driving industrial integration and economic growth.

Concurrent Events

Alongside the exhibition, a lineup of over 150 concurrent events will explore groundbreaking ideas and foster collaboration. These include:

The 7th China Green Economy Summit and Chinese Cities Investment Attracting Conference
Innovative Biological Drugs and Cell Quality Progress Forum
Molecular Diagnosis and Companion Diagnosis Summit Forum
Antibody Drugs and New Drug R&D Innovation Forum
Gene Sequencing Application Development Forum
Southern University of Science and Technology Forum
International Cross-domain Cooperation and Collaborative Development of Cross-border E-commerce Forum
China Silicon Photonics Industry Forum
AI Terminal, Intelligent Positioning System New Product Launch
2024 New Quality Productivity Summit

Unparalleled Market Access and Networking Opportunities:

Unmatched Exposure: To attract over 500,000 attendees, including 150 domestic and international delegations from 105 countries and regions.
Influential Audience: To engage with more than 10,000 technological projects and 5,000 exhibitors, including 800+ listed companies and 400+ CEOs and entrepreneurs from multinational corporations.
Media Reach: To gain extensive media coverage from over 1,500 journalists representing 200 domestic and overseas media organizations, ensuring global visibility.
Industry Leaders: To network with prominent figures such as Nobel Prize winners and top industry scholars, enhancing your brand’s credibility and influence.

CHTF is where global innovation converges, serving as a gateway to China’s booming tech market. It offers invaluable insights into market trends and fosters partnerships on a global scale, making it an unmissable event for anyone involved in the technology sector.

To register as an exhibitor, please visit here.

To register as a visitor, please visit here.

For more information, please visit www.chtf.com/english/

View source version on businesswire.com: https://www.businesswire.com/news/home/20240721948434/en/

Contacts

Media Cooperation
Ms. Ocean An
ah@zhenweiexpo.com

Booth Booking
Ms. Donna Hau
hjn@zhenweiexpo.com

Visitor Enquiry
Ms. Sarah Wang
sarah@zhenweiexpo.com

About Business Wire

For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.

www.businesswire.com

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

Corcept Announces CHMP Opinion Recommending EU Marketing Authorization for Lifyorli ® (Relacorilant)18.9.2026 15:00:00 EEST | Press release

Corcept Therapeutics Incorporated (NASDAQ: CORT), a commercial-stage company engaged in the discovery and development of medications to treat severe endocrinologic, oncologic, metabolic and neurologic disorders by modulating the effects of the hormone cortisol, today announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recommended that the European Commission (EC) should approve relacorilant, combined with the chemotherapy drug nab-paclitaxel, for the treatment of patients with platinum-resistant ovarian cancer. The CHMP’s recommendation is based on positive data from Corcept’s Phase 2 and pivotal Phase 3 ROSELLA trials, in which patients receiving relacorilant combined with nab-paclitaxel experienced improved progression-free and overall survival compared to patients who received nab-paclitaxel alone. The safety profile of relacorilant plus nab-paclitaxel in these trials was consistent with the safety profile of nab-paclitaxel monoth

Enhertu ® Recommended for Approval in the EU by CHMP as Adjuvant Treatment for Patients with Residual Disease After Neoadjuvant Treatment for HER2 Positive Early Breast Cancer18.9.2026 15:00:00 EEST | Press release

Enhertu® (trastuzumab deruxtecan) has been recommended for approval in the European Union (EU) as a monotherapy for the adjuvant treatment of adult patients with resected HER2 positive breast cancer who have residual invasive disease after neoadjuvant taxane-based and HER2 targeted treatment. Enhertu is a specifically engineered HER2 directed DXd antibody drug conjugate (ADC) discovered by Daiichi Sankyo (TSE: 4568) and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca (LSE/STO/NYSE: AZN). The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) based its positive opinion on results from the DESTINY-Breast05 phase 3 trial presented at the 2025 European Society for Medical Oncology (#ESMO25) Congress and subsequently published in The New England Journal of Medicine. The recommendation will now be reviewed by the European Commission, which has the authority to grant marketing authorizations for medicines in the EU. In DES

CHMP Recommends EU Approval of New Indication for Alfasigma’s Jyseleca ® (filgotinib), Treatment of Adults With Axial Spondyloarthritis18.9.2026 13:58:00 EEST | Press release

Alfasigma S.p.A, a global pharmaceutical company with a focus on innovation in rare disease and specialty care in areas where there is significant unmet patient need, today announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion for Jyseleca® (filgotinib), an oral, once-daily JAK1 preferential inhibitor, for the treatment of patients with active axial spondyloarthritis (axSpA), both non-radiographic and radiographic forms of the disease, who have responded inadequately to conventional therapy. Following this positive opinion, the application is now referred to the European Commission (EC) for final action. The EC’s decision is expected in the next weeks. “At present, half of people living with axSpA fail to adequately respond to treatment, leaving them with years of preventable struggle with persistent pain and other impactful symptoms,” said Daniele D'Ambrosio, Chief Development Officer, Alfasigma. “This

IMPACT Therapeutics and Pharmanovia Announce Positive CHMP Opinion for Senaparib, as a Potential First-Line Maintenance Treatment of Advanced High-Grade Epithelial Ovarian, Fallopian Tube, and Primary Peritoneal Cancer18.9.2026 13:38:00 EEST | Press release

For business and medical media only This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260918325771/en/ Stephan Eder, CEO, Pharmanovia IMPACT Therapeutics (07630.HK), a commercial-stage biotechnology company focused on the discovery and development of targeted anti-cancer therapeutics based on synthetic lethality mechanisms, together with global specialty pharmaceutical company Pharmanovia, today jointly announce that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending the granting of a Marketing Authorisation (MA) for the medicinal product Sepalna® (senaparib) intended for the maintenance treatment of advance epithelial ovarian, fallopian tube and primary peritoneal cancer. Following the CHMP’s recommendation for approval, senaparib will be submitted to the European Commission (EC) for final decision. Once approved by the EC, senaparib will

Estithmar Holding Announces Completion of 48.68% Stake Transfer in Shahba Bank to Masaref Holding, a Subsidiary of Estithmar Capital18.9.2026 12:48:00 EEST | Press release

Estithmar Holding Q.P.S.C. announced the completion of the transfer of a 48.68% stake in Shahba Bank to Masaref Holding LLC, subsidiary of Estithmar Capital, Estithmar Holding’s financial services and investments arm. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260918807909/en/ Estithmar Holding Announces Completion of 48.68% Stake Transfer in Shahba Bank to Masaref Holding, a Subsidiary of Estithmar Capital (Photo: AETOSWire) As a shareholder, Masaref Holding intends to support the assessment of proposals aimed at strengthening Shahba Bank’s financial, operational and technological capabilities, including potential capital enhancement, branch network expansion, and the development of products and services for individuals, businesses and SMEs. The proposals may include modernizing banking and operational systems, develop digital services, and strengthen governance, compliance, risk management and cybersecurity to enhance

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom