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BioWorld - Monday, August 3, 2026
Breaking News: Science fiction realized: BCI tech is hereBreaking News: Science fiction realized: BCI tech is here
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Samsung Bioepis stepping into EU market with Enbrel biosimilar

Jan. 20, 2016
By Haky Moon and Cornelia Zou
HONG KONG – South Korea's Samsung Bioepis Co. Ltd. got the first EU approval for biosimilar etanercept, a win that opens up the European market for a company that is working to become a global top-tier biosimilar maker.
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Experts: India too dependent on APIs imported from China

Jan. 20, 2016
By T.V. Padma
NEW DELHI – Pharmaceutical manufacturers and policy makers in India are growing increasingly concerned about the country's dependence on China as the single source for bulk drugs and intermediary products that are necessary to the production of a wide range of products.
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CFDA cracking down on clinical trials, urging greater oversight

Jan. 20, 2016
By Pearl Liu
HONG KONG – As part of an ongoing process of strengthening the country's drug regulatory structure, the CFDA is looking to end region-to-region variation in the strength of clinical trial oversight.
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Antifungal drug could prove answer to multidrug resistance

Jan. 20, 2016
By John Fox
HONG KONG — Chinese researchers have discovered that an antifungal drug can efficiently block bacterial virulence due to Staphylococcus aureus infections, including those caused by methicillin-resistant Staphylococcus aureus (MRSA) strains of the bacterium, in mouse models of infection, they reported in the Jan. 18, 2015, edition of Nature Chemical Biology.
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Daiichi, Coherus hit phase III marks for Enbrel biosimilar

Jan. 20, 2016
By Cornelia Zou
HONG KONG – Japanese pharma major Daiichi Sankyo Co. Ltd., looking to enter the biosimilar game, reported positive results from a co-developed drug that could become the country's first biosimilar etanercept.
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Other news to note

Jan. 19, 2016

Tianyin Pharmaceutical Inc., of Chengdu, China, received an acceptance letter from the NYSE MKT LLC exchange regarding a compliance plan to meet continued listing requirements. The company was notified of its noncompliance due to the delay in filing its quarterly report on Form 10-Q for the period ended Sept. 30, 2015, in addition to the delay in filing of its annual report on Form 10-K for the year ended June 30, 2015.


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India's multipronged 5-year strategy aims to boost biopharma sector

Jan. 13, 2016
By T.V. Padma
NEW DELHI – India plans to set up a new National Centre for Drug Discovery from Natural Products and strengthen its infrastructure and regulatory support for drugs trials, all part of its second national biotechnology research strategy unveiled recently.
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Canbridge confirms ligand CD95 in Chinese patient biomarker study

Jan. 13, 2016
By Shannon Ellis
SHANGHAI – Canbridge Life Sciences Inc. has confirmed the existence of ligand CD95 in Chinese glioblastoma patients after completing the first such biomarker study of its kind on the mainland. The study demonstrated a high degree of CD95 ligand expression consistency between geographically diverse Chinese and Western glioblastoma multiforme patients.
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China's biopharma execs convene at pre-JPM meeting in upbeat mood

Jan. 13, 2016
By Shannon Ellis
SAN FRANCISCO – While many of China's biopharmaceutical company executives flew across the Pacific for the J.P. Morgan Healthcare Conference, they kicked off the week with the Bayhelix 13th Annual Conference, a confab of China's best and brightest. The group's founding members were ambitious China-born scientists and managers working in the U.S. looking for camaraderie. Today, they are leaders in the field, heading up their own well-financed biopharma, med tech, service and investment companies.
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J&J expands efforts in HBV, inks partnership with China's CTTQ

Jan. 13, 2016
By Cornelia Zou
HONG KONG – Looking to further its innovative efforts in drug development, pharma major Johnson & Johnson has partnered with Chinese liver disease expert Chia Tai Tianqing Pharmaceutical Group Co. Ltd. (CTTQ), as well as a score of other external companies.
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