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The German Dusseldorf Medical Equipment Exhibition (MEDICA)

Organiser：MEDICA Time：November 17 – November 20, 2025 Address：ostfach 10 10 06, D-40001 Dusseldorf; Stockum Church Street 61, D-40474, Dusseldorf, Germany – D-40001 Exhibition hall：Dusseldorf Exhibition Center Product range: Medical Equipment: Medical electronic instruments, clinical laboratory analysis instruments, dental equipment and materials, hemodialysis equipment, respiratory equipment, hospital ward equipment, operating room equipment, emergency room equipment, hospital office equipment, etc. Imaging and Diagnostics: Ultrasound instruments, X-ray equipment, medical optical instruments. Disposable Consumables: Disposable medical supplies, dressings and hygiene materials, various surgical instruments, etc. Medical Devices: Healthcare equipment, home healthcare products, physical therapy equipment, orthopedic technology, etc. Medical Peripherals: Information and communication technology, medical services and publications, IT systems and IT solutions, etc. Laboratory Equipment Physical Therapy/Orthopedic Technology About MEDICA German： The German Dusseldorf Medical Equipment Exhibition (MEDICA) is the world’s largest and most authoritative exhibition for hospitals and medical equipment. It holds an unparalleled position in terms of scale and ...
- Source: drugdu
- 148
- November 13, 2025
Anke Biotech increases its investment in Boshengji and acquires exclusive national commercialization rights for its CD7-CAR-T cell therapy

　　China Securities Journal (Wang Luo) – On November 11, Anke Biotechnology…The company announced on its official WeChat account that it has signed a Capital Increase Agreement and an Exclusive Agency Framework Agreement with Boshengji Pharmaceutical Technology (Suzhou) Co., Ltd., establishing a new round of in-depth strategic cooperation. According to the agreements, Anke Biotechnology , as Boshengji’s second-largest shareholder, will invest an additional 30 million yuan to increase Boshengji’s capital. Simultaneously, Anke will leverage its commercial advantages to obtain the exclusive nationwide distribution rights for Boshengji’s core product, PA3-17 injection. This move marks a formal upgrade from early R&D cooperation and equity investment to a comprehensive strategic partnership based on “capital binding and joint business operation.” 　　This collaboration revolves around Boshengji’s core investigational product—PA3-17 injection, the world’s first Investigational New Drug (IND) approved product targeting CD7 autologous CAR-T cells. Developed independently by Boshengji Anke Cell Technology Co., Ltd., a wholly-owned subsidiary ...
- Source: drugdu
- 183
- November 12, 2025
Zhifei Biological’s subsidiary receives approval for clinical trials of its DPT vaccine for adolescents and adults

　　On November 11, Zhifei Biological Products Co., Ltd.(300122) issued an announcement stating that the company recently received approval from the National Medical Products Administration to allow its wholly-owned subsidiary to conduct clinical trials of its adsorbed acellular pertussis-diphtheria-tetanus (diphtheria-tetanus) combined vaccine (for adults and adolescents). 　　This vaccine aims to prevent infectious diseases such as diphtheria, tetanus, and pertussis, filling the market gap in domestic DPT (diphtheria, pertussis, and tetanus) vaccines for adolescents and adults. This approval marks a significant advancement for the company in vaccine development; the adolescent and adult DPT vaccine is a new generation of acellular vaccine, using separately purified active ingredients. 　　The company stated that if the clinical trials proceed smoothly, it will further enhance its market competitiveness, enrich its product line, and lay the foundation for long-term development. While this approval will not have a significant impact on near-term performance, future product development progress will improve ...
- Source: drugdu
- 109
- November 12, 2025
Increasing Market Supply of Influenza Vaccines; 48 Batches of Quadrivalent Influenza Virus Split Vaccine Have Been Released

　　Southern Finance, November 11th – According to CLS (China Lianhe Securities), from Hualan Biological…According to sources, as of now, the company has approved and released influenza vaccines in 2025.54 batches of vaccines have been released, including 48 batches of quadrivalent influenza virus split vaccine. Since October, and especially November, public awareness of influenza vaccination has increased significantly, and the demand orders from disease control centers across the country have increased significantly compared to the same period last year. The company is increasing its market supply of influenza vaccines and will expedite the transportation of vaccines nationwide through cold chain systems after receiving orders from disease control centers across the country to meet the vaccination demand. https://finance.eastmoney.com/a/202511113561078126.html
- Source: drugdu
- 241
- November 12, 2025
Bohui’s innovative freeze-dried Haemophilus influenzae type b conjugate vaccine clinical trial approved

　　On November 11th, Bohui Innovation(300318) issued an announcement stating that its controlling subsidiary, Langfang Bohui, and Baihui Biotechnology jointly applied for the development of freeze-dried influenza B virus.The Haemophilus influenzae conjugate vaccine has received a Drug Clinical Trial Approval Notice from the National Medical Products Administration, agreeing to conduct clinical trials. This vaccine is intended to prevent invasive infections caused by Haemophilus influenzae type b . The relevant application number is CXSL2500616, and the notification number is 2025LP02755. 　　The announcement states that drug development is characterized by high investment, high risk, and long cycles, and carries risks such as clinical trial results falling short of expectations and failure to obtain approval from relevant authorities. This receipt of the “Drug Clinical Trial Approval Notice” is considered a milestone in the development process and is not expected to have a significant impact on the company’s recent performance. 　　In the first three quarters ...
- Source: drugdu
- 127
- November 12, 2025
What diet do people with type 2 diabetes really want? Study reveals flexibility beats strict meal plans

British adults with diabetes overwhelmingly favor simple, adaptable eating patterns over rigid low-calorie meal replacements, highlighting that personal choice may be key to long-term adherence and better health outcomes. In a recent article published in the Journal of Human Nutrition and Dietetics, researchers investigated the dietary approaches preferred by British adults with type 2 diabetes (T2D) and the reasons behind these preferences. They found that most participants preferred moderately calorie-restricted or low-carbohydrate food-based diets, prioritizing ease of following instructions and simplicity as the most important qualities of an adequate diet. Relationship Between Type 2 Diabetes and Dietary Management T2D is closely linked with obesity and overweight, and dietary weight loss remains central to its management. However, many individuals struggle to adhere to prescribed diets due to barriers such as cultural food practices, social routines, and complex diet structures. Current UK Recommendations for Low Energy Diets In the UK, CLEDs, which ...
- Source: drugdu
- 102
- November 12, 2025
Utah researchers uncover microglia as key regulators of anxiety in the brain

Anxiety disorders are some of the most common mental health conditions in America, affecting about one in five people nationwide. But much remains unknown about the roots of anxiety in the brain. Now, research at the University of Utah has identified two surprising groups of brain cells in mice that act as “accelerators” and “brakes” for anxiety. Unexpectedly, the brain cells that regulate anxiety aren’t neurons, the cells that link together to make circuits and pass signals over long distances in the body. Instead, a kind of immune cell called microglia appears to fundamentally regulate whether mice are anxious or not. One group of microglia spurs anxiety responses; the other group tamps them down. “This is a paradigm shift,” says Donn Van Deren, PhD, postdoctoral research fellow at the University of Pennsylvania, who did the research as a postdoctoral research fellow in human genetics at University of Utah Health. “It ...
- Source: drugdu
- 145
- November 12, 2025
【EXPERT Q&A】How to apply for a business license for Class I medical devices?

Drugdu.com expert’s response: Class I medical devices do not require a license for business operations, but if production or specific sales activities are involved, a filing certificate is required. The specific application process is as follows: I. Filing Requirements for Business Operations of Class I Medical Devices Situations Requiring No License or Filing If an enterprise is solely engaged in the sales of Class I medical devices (without involvement in production), it only needs to explicitly include “sales of Class I medical devices” in its business scope on the business license, without the need for additional licenses or filings. Situations Requiring Filing Product Filing: If an enterprise sells self-produced Class I medical devices, it needs to submit filing materials to the local municipal drug regulatory authority (drug administration bureau) before the product is marketed, in order to obtain a “Filing Certificate for Class I Medical Devices”. Production Filing: If an ...
- Source: drugdu
- 139
- November 12, 2025
Phase II Clinical Trial Approved for 9MW3811 Injection in Pathological Scarring

On November 10, Maiwei Biotechnology (688062) issued an announcement stating that the company recently received the “Drug Clinical Trial Approval Notice” issued by the National Medical Products Administration, which approved the application for Phase II clinical trial of 9MW3811 injection for the indication of pathological scars. The clinical trial notification number for this drug is 2025LP02967. The approval conclusion shows that it meets the relevant requirements for drug registration and allows clinical trials to be conducted. 9MW3811 is a humanized monoclonal antibody targeting human IL-11 independently developed by the company. It has high target affinity and signal blocking ability and is expected to demonstrate efficacy in various diseases such as pathological scars and pulmonary fibrosis. The company plans to launch its Phase II clinical trial for pathological scars by the end of 2025 and has entered into an exclusive licensing agreement with CALICO LIFE SCIENCES LLC. CALICO has already paid ...
- Source: drugdu
- 174
- November 11, 2025
Gan & Lee Pharmaceuticals and Hillhouse Capital have reached a strategic cooperation agreement to optimize resource allocation and explore cooperation opportunities.

Shanghai Securities News China Securities(Reporter Zhang Xue) On November 10, Gan & Lee Pharmaceuticals…The company announced the transfer of its controlling stake in its wholly-owned subsidiary, GanGan Medical Technology Jiangsu Co., Ltd. (hereinafter referred to as “GanGan Jiangsu”), to Hillhouse Capital. Founded in 2017, GanGan Jiangsu is an innovation-driven medical technology company specializing in the research and development and production of high-quality drug delivery devices. Leveraging its strong pharmaceutical background and rigorous quality system, the company has established a comprehensive quality management and regulatory compliance system that meets international standards. Its products have obtained certifications from the U.S. Food and Drug Administration (FDA) and the European Union’s CE MDR (European Union Medical Device Registration System).(Regulations) certification. As the transferee, Hillhouse Capital has long focused on investments in the healthcare sector, possessing comprehensive industry chain insights and resource integration capabilities. Leveraging Hillhouse’s extensive experience in healthcare industry operations and value enhancement, ...
- Source: drugdu
- 188
- November 11, 2025

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