Health Tech Speed Clinic – in collaboration with Institute of Systems Science, NUS
Everyone’s gone to a clinic at some point in time […]
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Class III Medical Device Manufacturer’s GMP Certification – Beijing Municipal Food and Drug Administration
The Beijing Municipal Food and Drug Administration rele
Access-2-Healthcare偕同台湾工研院对台湾医疗技术行业普及ISO13485：2016更新内容
一切都是从一场双方友好地交谈开始，逐渐发展成为台湾工研院与 Access-2-Healthcare 之间更多正
Access-2-Healthcare偕同台湾工研院对台湾医疗技术行业普及ISO13485：2016更新内容 閱讀全文 »
Access-2-Healthcare partners with Industrial Technology Research Institute of Taiwan to help Taiwan medical technology organisations understand ISO13485:2016
What began as a friendly conversation between two bloke
QUALITY MANAGEMENT REGULATIONS FOR MEDICAL DEVICE CLINICAL TRIALS
On March 23, 2016, the CFDA has released its Quality Ma
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ADVERSE EVENTS MONITORING REPORT FOR YEAR 2015 – CHINA FDA
On May 27, 2016, the China Food and Drug Administration
ADVERSE EVENTS MONITORING REPORT FOR YEAR 2015 – CHINA FDA 閱讀全文 »
Release for Public Comment – Registration Requirements for Innovative Medical Devices – China FDA
“The Requirements of Application Materials for Special
New Consultation Guidelines from Center of Medical Device Evaluation (CMDE)
The Center of Medical Device Evaluation (CDE) released
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List of Clinical Trial Exempt Devices – Updated List by China Food and Drug Adminisration (CFDA)
The China Food and Drug Administration released the dra
Access-2-Healthcare Partners with Rob Jelas Regulatory Training & Assistance to Help New Zealand manufacturers Understand ISO13485:2016
“Since New Zealand gets the first rays of sunlight, why