2021 |
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07 |
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Mass Production of Triple-Injection Synovial Fluid Supplement in the Biotech Plant 1
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2020 |
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04 |
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Absorbable Nasal Dressing Launched
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05 |
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Mass Production of Single-Injection Synovial Fluid Supplement in the Biotech Plant 1
HYAJOINT Plus Synovial Fluid Supplement is Approved by Pricing System for Pharmaceuticals (Single Injection per Year) under the Scheme of Taiwan National Health Insurance System
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07 |
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Stablized Synovial Fluid Supplement Launched
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09 |
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HYAJOINT Synovial Fluid Supplement is Approved by TFDA for the New Indication of Shoulder Rotator Cuff Lesions without Complete Tears
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11 |
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Approval of HALAL Assurance System (HAS)
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12 |
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PROTAHERE Absorbable Adhesion Barrier Won the Silver Award in “2020 Research and Development of Pharmaceutical Technology Award”
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2019 |
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06 |
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Awarded with the "16th the National Brand YuShan Award" as an Outstanding Enterprise
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07 |
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Sodium Hyaluronate Facial Dermal Implant with Lidocaine in Gel Type Launched
The Biotech Plant 1 is ISO 13485 Certified
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08 |
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The Biotech Plant 1 is GMP Certified for the Class Ⅲ Medical Device by the Ministry of Health and Welfare, Republic of China (Taiwan)
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2018 |
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08 |
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DEFEHERE Absorbable Adhesion Barrier Launched in Taiwan
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09 |
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Sodium Hyaluronate Facial Dermal Implant with Lidocaine is CE-MDD 93/42/EEC (ClassIII) Certified and Obtained the CE Marking
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2017 |
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01 |
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Sodium Hyaluronate Intravesical Instillation Launched
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02 |
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PROTAHERE Absorbable Adhesion Barrier Launched
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03 |
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European Patent for the Technique of Cross-linked Hyaluronic Acid Platform (CHAP) Granted
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06 |
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Approval of Sedex Members Ethical Trade Audit (SMETA)
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2016 |
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05 |
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Sodium Hyaluronate Wound Repair Hydrogel Launched
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06 |
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U.S. Patent for the Technique of Cross-linked Hyaluronic Acid Platform (CHAP) Granted
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08 |
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Signed an Exclusive Distribution Agreement with GALDERMA S.A. (Subsidiary of Nestlé)
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2015 |
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10 |
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Approval of Subsidy Project of Investing Development and Promoting Industry from the Kaohsiung City Government
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2014 |
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04 |
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Sodium Hyaluronate Facial Dermal Implant Launched in China
Passed the GMP Inspection by Korea Competent Authority
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05 |
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Approval of Canadian Medical Devices Conformity Assessment System (CMDCAS) Certification
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2013 |
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03 |
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Taiwan Patent for the Technique of Cross-linked Hyaluronic Acid Platform (CHAP) Granted
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11 |
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Japan Patent for the Technique of Cross-linked Hyaluronic Acid Platform (CHAP) Granted IPOs (Initial Public Offerings) Launched in Taiwan
Sodium Hyaluronate Facial Dermal Implant with Lidocaine Launched
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12 |
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Approval of Taiwan Intellectual Property Management System (TIPS) Certification
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2012 |
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02 |
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Single-Injection Synovial Fluid Supplement Launched
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10 |
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Awarded with the “National Industry Innovation Award” from the Ministry of Economic Affairs
Awarded with the “National New Innovation Award” from the Institute for Biotechnology and Medicine Industry
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2011 |
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05 |
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Sodium Hyaluronate Hydrogel Wound Dressing Launched
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06 |
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Sodium Hyaluronate Facial Dermal Implant Launched in Korea
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12 |
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China Patent for the Technique of Cross-linked Hyaluronic Acid Platform (CHAP) Granted
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2010 |
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02 |
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Sodium Hyaluronate Facial Dermal Implant Launched
Triple-Injection Synovial Fluid Supplement Launched in Philippines
Sodium Hyaluronate Facial Dermal Implant Launched in Italy
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12 |
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Listed on the Taipei Exchange (TPEx) with Emerging Stock Market Code 1786
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2009 |
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01 |
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Sodium Hyaluronate Facial Dermal Implant Launched in India
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02 |
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Program for Development of New Leading Products, Facial Dermal Implant of Crosslinked Hyaluronan, was Approved by the Industrial Development Bureau, Ministry of Economic Affairs
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05 |
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Listed as Biotech and New Pharmaceutical Industry by the Industrial Development Bureau, Ministry of Economic Affairs
The ITDP-Fast Track for Clinical Trial Program, Sodium Hyaluronate Facial Dermal Implant Clinical Trial Project, was Approved by the Ministry of Economic Affairs
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08 |
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The Small Business Innovation Research (SBIR), Single-Injection Synovial Fluid Supplement R&D Project, was Approved by the Kaohsiung City Government
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2008 |
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08 |
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Triple-Injection Synovial Fluid Supplement Launched
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12 |
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HYAJOINT Synovial Fluid Supplement was Awarded the “National Biomedical Quality Award”
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2006 |
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01 |
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The Export Permit for HYADERMIS Facial Dermal Implant was Issued by the Department of Health, Executive Yuan. Registration No. DOH-MD-(E)-No. 000028
The Export Permit for HYAJOINT Synovial Fluid Supplement was Issued by the Department of Health, Executive Yuan. Registration No. DOH-MD-(E)-No. 000029
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08 |
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Triple-Injection Synovial Fluid Supplement Launched in India
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2005 |
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01 |
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Achieved the ISO 9001 and ISO 13485 Certification for Medical Device Quality Management System
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03 |
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Sodium Hyaluronate Facial Dermal Implant was CE-MDD 93/42/EEC (Class III) Certified and Obtained the CE Marking
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07 |
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Awarded with the “Product Innovation Leadership Award of the Biomedical Material Category” from the Frost & Sullivan Awards.
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09 |
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The Medical Device Plant was GMP Certified for the Class Ⅲ Medical Device by the Department of Health, Executive Yuan
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12 |
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Sodium Hyaluronate Synovial Fluid Supplement was CE-MDD 93/42/EEC (Class III) Certified and Obtained the CE Marking
Awarded with the “Export Processing Zone Innovative Research and Development Award” from the Ministry of Economic Affairs
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2004 |
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09 |
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Awarded with the “Investment Incentive Program” from the Kaohsiung City Government
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2003 |
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03 |
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Achieved the CNLA Certification (The First Certified Parentage Testing Laboratory in Taiwan).
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12 |
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Program for Development of New Leading Products, Medical Grade Hyaluronic Acid, was Approved by the Ministry of Economic Affairs
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2002 |
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10 |
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Achieved the ISO 9001 Certification
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