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BioWorld - Thursday, December 11, 2025
Home » regulatory

Articles Tagged with ''regulatory''

South Korea improves innovative medical device policies, but more needed

Dec. 31, 2019
By Jihyun Kim
HONG KONG – Aiming to attract more active innovation to its medical device industry, South Korea updated some of its industry regulations through 2019. The ultimate goal was to make it easier for advanced medical technologies that use artificial intelligence (AI), robotics and 3D printing that have yet to penetrate the market due to inefficient approval processes.
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China three-year plan aims to put patient access to cancer drugs on par with other markets

Oct. 2, 2019
By Elise Mak
SUZHOU, China – Under the "Healthy China" campaign, China has introduced a three-year action plan for preventing and treating cancer. The plan vows to speed up the marketing of cancer drugs in the country, even aiming for simultaneous marketing with other countries.
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IP enforcement in China improving slowly but surely

Sep. 25, 2019
By Mark McCarty

China's state machine is set to drive innovation, but needs more than just drug law reforms

Sep. 25, 2019
By Elise Mak
SUZHOU, China – A recent revision to China's legal infrastructure for the pharma industry represents a concrete step toward bolstering domestic biotech innovation, said stakeholders gathered at last weekend's China Biomed Innovation and Investment Conference.
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More approvals by FDA: Rare disease, oncology and HKEX remain the focus

Sep. 25, 2019
By Elise Mak
SUZHOU, China – The global biotech market continues to look promising and Chinese companies are taking notice as they lay the foundation for new advances.
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FDA lays framework for engaging patients in device clinical trials

Sep. 24, 2019
By Meg Bryant
BOSTON – The FDA's Center for Device and Radiological Health (CDRH) released draft guidance on Monday aimed at encouraging the use of patient input in medical device clinical trials and helping sponsors understand how they can use patient engagement to improve the design and conduct of investigations.
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FDA sustains guidance deluge with draft for conformity assessment

Sep. 23, 2019
By Mark McCarty
The FDA's Center for Devices and Radiological Health has released yet another draft guidance dealing with medical device premarket programs with the release of a draft guidance for the accreditation scheme for conformity assessment. The draft frequently references independent standards for assessing device performance and safety, thus bringing regulatory harmonization one step closer to a practicable reality.
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Product regulatory actions for Sept. 19, 2019

Sep. 20, 2019

FDA resets performance guidance along with four product-specific guidances

Sep. 20, 2019
By Mark McCarty

FDA unveils expedited review program for safer medical devices

Sep. 19, 2019
By Mark McCarty
The U.S. FDA's emphasis on device safety is well known. Now, the agency has published a draft guidance that aims to provide expedited reviews for device and diagnostic applications that are "reasonably expected to significantly improve" safety, which, in conjunction with the breakthrough devices program, suggests that many other applications will be in the queue for increasingly longer periods of time.
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