Ministry of Science and Technology of the People´s Republic of China published the new administration process of human genetic resources in clinical trial in the end of October.
More On October 9, 2017, Medical Device Authority (MDA) Malaysia released a Second Edition of the Guidance Document on Change Notification for Registered Medical Device. This GD serves a great purpose in informing the stakeholders on the categories of changes, notification process and relevant requirements for applying for a change notification in Malaysia.
More Qualtech and Croma (Austria) are currently under GCP inspection by CFDA in Sichuan Clinical Trial Institutions. The latest information will be posted up-to-date!
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