Polarean Imaging plc (AIM: POLX), a provider of advanced Magnetic Resonance Imaging (MRI) for lung function, announced on Monday that it has signed its first distribution agreement with Sumtage Enterprise Company Limited for the distribution of its Xenon MRI platform in Taiwan.
This deal marks a significant step in expanding Polarean's international presence.
Polarean will collaborate with Sumtage to secure the necessary regulatory approvals for the commercial launch of its innovative Xenon MRI technology in Taiwan. Sumtage, a medical distributor with 30 years of experience, will provide ongoing support and maintenance services for the product.
Headquartered in Durham, NC, and London, UK, Polarean is revolutionising pulmonary medicine by offering non-invasive, radiation-free imaging solutions. Its flagship product, XENOVIEW, the first FDA-approved hyperpolarised Xenon MRI inhaled contrast agent, is designed to meet the needs of over 500 million patients globally suffering from chronic respiratory diseases.
Polarean Imaging expands reach with Taiwanese distribution deal
AstraZeneca secures EU recommendation for Imfinzi in limited-stage small cell lung cancer
CHMP recommends EU approval of Daiichi Sankyo and AstraZeneca's datopotamab deruxtecan
Renalys Pharma completes patient enrolment for Phase III clinical trial of sparsentan
NICE recommends ALK's ACARIZAX for house dust mite allergic rhinitis treatment in UK's NHS
Roche's blood test measuring Lp(a) in molar units receives US FDA 510(k) approval
Breckenridge Pharmaceutical's Everolimus Tablets for Oral Suspension receive US FDA approval
Amgen's BLINCYTO (blinatumomab) monotherapy approved in Europe
HeartBeam submits FDA 510(k) application for groundbreaking 12-lead ECG synthesis software
FDA grants Vicore Pharma Fast Track Designation for buloxibutid in idiopathic pulmonary fibrosis
FDA accepts Saol Therapeutics' SL1009 New Drug Application for Priority Review
FDA grants Regenerative Medicine Advanced Therapy designation to Beacon Therapeutics' laru-zova
AstraZeneca and Daiichi Sankyo's Enhertu approved in US for earlier treatment of breast cancer
ImmunityBio's ANKTIVA receives EMA review for BCG-unresponsive bladder cancer treatment