Imagion Biosystems Reports Progress on Regulatory Pathway
Following FDA guidance for medical devices, Imagion filed a Pre-Submission document with the FDA in January 2018 to initiate communications regarding the Company's clinical development plans. Pre-Submissions are optional filings with the FDA but are encouraged, particularly for new technology medical products, to foster open communication and dialog with the agency. The FDA provides written feedback on Pre-Submissions within 3 months, which the Company recently received, confirming key aspects of the Company's development plan:
Key next steps in the development process required before first-in-human testing include:
Imagion Biosystems is at the crossroads of biotechnology and nanotechnology. Its novel bioimaging and nanomagnetic detection systems have been developed specifically to detect cancer earlier and with higher specificity than is currently possible. With MagSense™ technology, the company has the potential to optimize patient care and reduce mortality rates across various cancer indications. Imagion Biosystems listed on the Australian Securities Exchange (ASX) in June 2017. For further information please visit www.imagionbiosystems.com
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SOURCE Imagion Biosystems
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