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MEDICALL EXPO

Organiser: Messe Düsseldorf GmbH (Germany) Time：September 19-21, 2025 address：Plot No. 25, 27, 28, 29, Knowledge Park II, Greater Noida, Uttar Pradesh 201306 or 201308, India Exhibition hall：Greater Noida Product range: Medical Technology/Electronic Medical Products, Equipment, and Systems Exhibition Area Diagnostic and Imaging Products, Equipment, and Systems Exhibition Area Portable Physical Therapy and Orthopedic Products, Equipment, and Systems Exhibition Area Surgical Products, Equipment, and Systems Exhibition Area Hygiene and Disinfection Products, Disposable Supplies Exhibition Area Medical Technology/Electronic Medical Products, Equipment, and Systems Exhibition Area Diagnostic and Imaging Products, Equipment, and Systems Exhibition Area Portable Physical Therapy and Orthopedic Products, Equipment, and Systems Exhibition Area Surgical Products, Equipment, and Systems Exhibition Area Hygiene and Disinfection Products, Disposable Supplies Exhibition Area Rehabilitation Devices and Equipment Exhibition Area About MEDICALL EXPO： The MEDICALL EXPO India is one of the most professional medical equipment exhibitions in India and South Asia. Organized by Messe ...
- Source: drugdu
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- September 16, 2025
Novartis and Monte Rosa Therapeutics Announce $5.7 Billion Licensing Agreement Deal for Protein Degraders

Novartis announced a licensing agreement with Monte Rosa Therapeutics valued upwards of $5.7 billion that aims at developing drugs for immune-mediated diseases. “We are pleased to expand our collaboration with Monte Rosa Therapeutics, building on the strong foundation and progress established through the VAV1 program,” said Fiona Marshall, Ph.D., president of biomedical research at Novartis. “This new agreement underscores our commitment to advancing targeted protein degradation as a promising approach to address immune-mediated diseases with high unmet need. We believe Monte Rosa’s QuEEN platform has the potential to uncover new insights in this field. We look forward to working together to translate these insights into transformative therapies for patients.”2 What are the details of the deal? Under the terms of the agreement, Novartis will pay Monte Rosa an upfront payment of $120 million (along with holding the potential to earn milestone payments and royalties), which brings the total to $5.7 ...
- Source: drugdu
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- September 16, 2025
Bariatric Fusion Vitamins Pulled for Missing Child-Safe Caps

MONDAY, Sept. 15, 2025 (HealthDay News) — About 4,700 bottles of Bariatric Fusion iron-containing multivitamins have been recalled because packaging does not meet federal safety standards, according to the U.S. Consumer Product Safety Commission (CPSC). The bottles, sold online at Amazon.com, bariatricfusion.com and other sites between January and June 2025, were made without child-resistant caps. Without this protection, children could open the bottles and swallow the vitamins, which contain high levels of iron. Accidental iron poisoning in children can cause serious injury or death. The recall involves: High ADEK multivitamin capsules (90- and 270-count bottles) One Per Day bariatric multivitamin capsules (90-count bottle) All recalled bottles contain 45 mg of iron and can be identified by lot numbers 0066J4, 0065J4, 0453B5 or 0370B5, printed on the bottom. Only bottles with smooth caps (no “push down & turn” embossing) are part of the recall. So far, no injuries have been reported, ...
- Source: drugdu
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- September 16, 2025
Smoking raises the risk of all subtypes of type 2 diabetes

The characteristics of type 2 diabetes vary from patient to patient and it has been proposed that the condition is made up of four subtypes. Now, new research being presented at the annual meeting of the European Association for the Study of Diabetes (EASD) in Vienna, Austria (15-19 September) shows that smoking increases the risk of the condition, regardless of subtype. The researchers in Sweden, Norway and Finland also found that people with a genetic susceptibility to develop diabetes seem more vulnerable to the adverse effects of smoking. It has previously been suggested that type 2 diabetes (T2D) can be divided into the following subtypes: SIRD (severe insulin-resistant diabetes), characterised by insulin resistance (where the body’s cells don’t respond to properly to insulin and can’t easily take up glucose from the blood); SIDD (severe insulin-deficient diabetes), characterised by a lack of insulin; MOD (mild obesity-related diabetes), associated with obesity and ...
- Source: drugdu
- 133
- September 15, 2025
Types, Triggers And New Treatments

SUNDAY, Sept. 14, 2025 (HealthDay News) — Everyone gets headaches, but not all headaches are the same. For some, they’re a quick inconvenience. For others, they can be intense, long-lasting and even disabling, disrupting daily life for days or weeks. Experts say finding the right treatment depends on identifying the type of headache and understanding what triggers it. “We define chronic headache as having more than 15 headache days per month. So, more days with headache than not,” Michael Oshinsky, a pain expert at the National Institutes of Health (NIH), told its monthly newsletter News In Health. The most common kind is a tension-type headache, often linked to stress, lack of sleep, dehydration or poor posture. Pain usually feels mild to moderate and affects both sides of the head. Migraines are another frequent cause of disabling pain. Unlike tension headaches, migraines are a complex brain condition that can cause: Severe ...
- Source: drugdu
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- September 15, 2025
Dobutamine Hydrochloride Injection Passes Consistency Evaluation

On September 13, Chengyi PharmaceuticalAn announcement was released regarding the company’s drug passing the generic drug consistency evaluation. The announcement revealed that the company recently received the “Notice of Approval of Supplementary Drug Application” from the National Medical Products Administration (NMPA). The company’s dobutamine hydrochloride injection has passed the generic drug quality and efficacy consistency evaluation. The drug is available in two strengths: 2ml: 20mg and 5ml: 100mg, both of which have been approved. Dobutamine hydrochloride injection is primarily used for the short-term supportive treatment of heart failure caused by organic heart disease and post-cardiac surgery low-output syndrome. The company received the Drug Registration Approval for dobutamine hydrochloride injection (2ml:20mg) from the National Medical Products Administration (NMPA) in September 2002. In July 2024, the company submitted an application for domestic production consistency evaluation of the drug to the NMPA’s Center for Drug Evaluation, also seeking an additional 5ml:100mg strength. The ...
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- September 15, 2025
“Pharma leader ” changes! Hengrui Medicine, don’t panic

Recently, Hengrui Medicine lost its position as the “No. 1 pharmaceutical company”. In the pharmaceutical industry, BeiGene’s transcendence sends a signal. For a long time in the past, Hengrui Medicine was the undisputed leader in the pharmaceutical industry. Relying on the model of “imitation + innovation”, Hengrui has been leading the entire industry, and many of its core products once occupied half of the domestic pharmaceutical market. As early as 2021, Hengrui Medicine’s stock price continued to rise after a series of sharp increases, reaching a high of 96.7 yuan per share, and its total market value reached an astonishing 616.9 billion yuan.However, the turning point also occurred in 2021. Affected by multiple factors in the industry and the outside world, Hengrui Medicine’s growth engine gradually stalled, and the “imitation + innovation” model began to fail. In terms of performance, from 2021 to 2023, Hengrui Medicine’s revenue growth rate was ...
- Source: drugdu
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- September 15, 2025
Is Sinovac Biotech’s controlling shareholder cashing out ahead of its Hong Kong IPO? Keyi Pharmaceuticals announces another 5% stake reduction plan, adding to its previous multiple reductions this year.

On September 14, Sinovac BiotechSinovac Biotech Co., Ltd. (hereinafter referred to as ” Sinovac Biotech ” or “the Company”) issued a shareholder inquiry transfer plan.The shareholder of the pre-IPO shareholder inquiry transfer (hereinafter referred to as “this inquiry transfer”) is Shenzhen Keyi Pharmaceutical Holdings Co., Ltd. (hereinafter referred to as “Keyi Pharmaceutical” or “the transferor”); the total number of shares to be transferred by the transferor is 10,062,800 shares, accounting for 5.00% of the company’s total share capital; this inquiry transfer is a non-public transfer, not conducted through centralized bidding or block trading, and does not belong to a reduction in holdings through the secondary market. The transferee shall not transfer the shares acquired through the inquiry transfer within 6 months after the acquisition. It is worth noting that Keyi Pharmaceutical has recently reduced its holdings of Sinovac Biotech shares through centralized bidding and block trading.Cashing out. The company’s net ...
- Source: drugdu
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- September 15, 2025
Autoimmune bispecific antibody product CS2015 selected for exhibition at the ACAAI Annual Meeting in the United States

On the morning of September 15th, CStone Pharmaceuticals (02616), a subsidiary of Zhongzheng Intelligent Finance , announced that its autoimmune and inflammatory drug candidate, CS2015 (OX40L/TSLP bispecific antibody), has been selected for presentation at the 2025 American College of Allergy, Asthma, and Immunology (ACAAI) Annual Scientific Meeting. The meeting will be held in Orlando, USA, from November 6th to 10th.　　CS2015 is a potential first-in-class/best-in-class bispecific antibody that simultaneously targets OX40L and TSLP. By dually inhibiting key regulators of Th2-mediated inflammatory responses, it provides a new treatment strategy for type 2 inflammatory diseases such as atopic dermatitis, asthma, and chronic obstructive pulmonary disease. CStone Pharmaceuticals is an innovation-driven biopharmaceutical company focused on drug research and development in key disease areas such as oncology, autoimmunity, and inflammation. Since its establishment, it has successfully launched four innovative drugs., and obtained approval for 16 new drug applications. The current R&D pipeline includes 16 drug ...
- Source: drugdu
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- September 15, 2025
【EXPERT Q&A】What certifications are required for the export of medical devices and pharmaceutical products?

Drugdu.com expert’s response: Medical devices and pharmaceutical products require multiple certifications for export based on the requirements of target markets, covering international standards, regional regulations, and special product specifications. Below is a detailed explanation: I. International General Certifications ISO Certifications ISO 13485: An international standard for the quality management system of medical devices, serving as a foundational certification for exports. It proves that a company’s production processes comply with international norms. ISO 9001: A general quality management system certification. While not mandatory, it enhances corporate credibility. GMP Certification Good Manufacturing Practice certification ensures that production processes meet international standards, particularly for pharmaceutical-grade medical devices (e.g., vaccines, injectables). II. Regional Mandatory Certifications EU Market CE Certification: The “passport” for entering the EU market, classified by risk level: Class I low-risk products (e.g., surgical scalpels): Require a CE Declaration of Conformity. Class I*, IIa, IIb, and III high-risk products (e.g., implantable devices, pacemakers): Require ...
- Source: drugdu
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- September 15, 2025

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