Wesper Revolutionizes Sleep Apnea Diagnosis with FDA-Cleared, Cannula-Free Technology
Without capturing this core signal, critical events like hypopneas can be missed, misclassified, or misunderstood. As clinical research and expert consensus increasingly affirm, airflow isn't optional—it's essential.
Global Pharma | 16/05/2025 | By Manvi | 265
Marksans Pharma's UK Subsidiary Relonchem Secures Marketing Authorisation for Gabapentin from UKMHRA
Relonchem Ltd. has received marketing authorisation for its product Gabapentin 50 mg/ml oral solution.
Global Pharma | 15/05/2025 | By Manvi | 259
Sanofi to Invest USD 20 Billion in US by 2030 to Expand R&D and Manufacturing
Sanofi has announced plans to invest at least $20 billion in the United States by 2030, significantly boosting R&D and manufacturing to support the launch of new therapies and strengthen the domestic supply chain.
Global Pharma | 15/05/2025 | By Manvi | 181
Genesys Spine Launches Stasys-C 3DP, a Zero-Profile 3D-Printed Cervical Standalone System
Genesys Spine has announced the commercial launch of the Stasys-C™ 3DP Cervical Standalone System, a 3D-printed, zero-profile cervical interbody solution designed to simplify anterior cervical procedures while promoting early fusion.
Global Pharma | 15/05/2025 | By Manvi | 178
Cariflex Inaugurates World's Largest Polyisoprene Latex Plant in Singapore
With an investment of USD 355 million, the plant is the largest of its kind in the world and will significantly expand Cariflex's production capacity to meet the growing demand for high-quality synthetic latex for medical and protective applications.
Global Pharma | 15/05/2025 | By Manvi | 446
Standard Glass Lining Technology (SGLTL) in collaboration with Japan’s AGI Group and its affiliate GL HAKKO will manufacture glass-lined shell and tube heat exchangers in India. The production is estimated to commence by Q4, FY26.
Global Pharma | 14/05/2025 | By Manvi | 671
Zydus Secures EIR from USFDA for Ambernath API Manufacturing Facility
Zydus Lifesciences has received an establishment inspection report (EIR) from the United States Food and Drug Administration (USFDA). The EIR has been classified under the no action indicated (NAI) category.
Global Pharma | 14/05/2025 | By Manvi | 390
USFDA Completes Inspection at Solara's Ambernath Facility with Zero Form 483 Observations
Solara Active Pharma Sciences Ltd. announced that its Ambernath API manufacturing facility has successfully completed a USFDA inspection with zero Form 483 observations, confirming the site’s compliance with regulatory standards.
Global Pharma | 14/05/2025 | By Manvi | 494
CuraTeQ Biologics Secures Approval for Biosimilar Zefylti from UK's MHRA
Aurobindo Pharma announced that its subsidiary CuraTeQ Biologics has received UK MHRA approval for Zefylti, a filgrastim biosimilar for treating neutropenia, marking its second MHRA-approved biosimilar.
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Global Pharma | 14/05/2025 | By Manvi | 443
Caplin Steriles Receives USFDA Approval for Haloperidol Decanoate Injection
Caplin Steriles Ltd., a subsidiary of Caplin Point Ltd., gets an entry into the US market with the final approval from Abbreviated New Drug Application (ANDA) for Haloperidol Decanoate Injection.
Global Pharma | 14/05/2025 | By Manvi | 388
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