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Leading Cervical Cancer Doctors Support Approval of LuViva in China Based on Preliminary Review of Clinical Trial Results

PEACHTREE CORNERS, Ga., February 20, 2024 Guided Therapeutics, Inc. (OTCQB: GTHP), the maker of the LuViva Advanced Cervical Scan, announced today that a group of prominent cervical cancer doctors are in the final stages of completing the clinical data report that will be submitted for approval by the Chinese National Medical Products Administration (NMPA). The data quality assurance review team is being led by Dr. Sui Long, Director of the Gynecology Hospital at Fudan University and includes p

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Guided Therapeutics Announces Completion of Clinical Study for Chinese Regulatory Approval

Guided Therapeutics Provides Update on Start of Clinical Trial for US FDA Approval

Guided Therapeutics, Inc. or the “Company” , the maker of LuViva, a rapid and painless cervical cancer detection system based on the Company’s patented biophotonic technology,. | May 1, 2023

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Guided Therapeutics (GTHP) Enters Agreement to Begin Clinical Trial for US FDA Approval

Guided Therapeutics (GTHP) Enters Agreement to Begin Clinical Trial for US FDA Approval
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Guided Therapeutics Signs Agreement to Begin Clinical Trial for US FDA Approval

Guided Therapeutics Signs Agreement to Begin Clinical Trial for US FDA Approval
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