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BioWorld - Friday, December 26, 2025
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Regulatory front for July 10, 2020

July 10, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Synthes.
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Harbour Biomed closes $102.8M series C to advance late-stage programs

July 10, 2020
By Elise Mak
BEIJING – Known for its transgenic mouse platforms to develop antibodies, U.S., China and the Netherlands-based Harbour Biomed Therapeutics Ltd. closed a series C funding round July 9 to raise $102.8 million to advance its late-stage clinical programs and COVID-19 pipeline.
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Fujifilm makes inroads for Avigan after tying up agreement with Dr. Reddy’s and GRA

July 10, 2020
By Gina Lee
HONG KONG – Tokyo-headquartered Fujifilm Holdings Corp. will increase production of Avigan on the back of a partnership with India’s Dr. Reddy’s Laboratories Inc. and Dubai-based Global Response Aid, an affiliate of logistics company Agility.
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Coronavac product packaging

China's Sinovac phase III trials in Brazil could take as little as three months

July 10, 2020
By Sergio Held and Elise Mak
CAJICA, Colombia, and BEIJING – Last week Sinovac Biotech Ltd., of Beijing, announced the approval by Anvisa, the Brazilian health care surveillance agency, to start phase III trials to test the efficacy and safety of its inactivated COVID-19 vaccine being developed by Sinovac Life Sciences, a subsidiary of the Chinese company, in the Latin American country.
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Other news to note for July 10, 2020

July 10, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: ATAI, Kures, Milliporesigma, Merck KGaA, Oragenics, Precigen.
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In the clinic for July 10, 2020

July 10, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Abeona, Atox, Center Laboratories, DBV, Gilead, Macrogenics, Sedana, Sosei, Tonix, Ziopharm.
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Product image

Philips, Biointellisense partner on at-home patient wearable to monitor COVID, chronic disease

July 9, 2020
By Stacy Lawrence
Biointellisense Inc. received an FDA clearance in January for its Biosticker to monitor patient vital signs at home for as long as 30 days. It was just starting to launch, when along came the novel coronavirus. Now, the Band-Aid-sized monitor is being used to monitor COVID-19 patients at home, as well as chronic disease patients.
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FDA icons

Real-world data coming into its own despite bad reputation in times gone by

July 9, 2020
By Mark McCarty
The use of real-world data (RWD) and real-world evidence (RWE) in regulatory decision-making may seem more aspirational than practical at times, but that state of affairs is changing rapidly. Wendy Rubenstein, director of personalized medicine at the U.S. FDA’s Center for Devices and Radiological Health, said contemporary versions of these real-world sources of evidence “are of progressively higher quality” in recent years, and thus RWE and RWD may soon hit their strides as mature sources of data with which regulators are increasingly comfortable.
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Asia at night from space

Hong Kong’s med-tech sector looks to leverage technology, funding to expand

July 9, 2020
By Bryan Wong
HONG KONG – Hong Kong’s emerging med-tech sector is getting a boost from a government-funded program aimed at sharing technology with other jurisdictions, a program driven in part by the need to contain the COVID-19 pandemic and continue opening regional economies.
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Regulatory front for July 9, 2020

July 9, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: MedPAC, Neovasc.
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