Chinese Government’s Evaluation Process Of Manufacturers’ Standards And Qualifications For Relevant Epidemic Prevention Products
View a flow chart of the evaluation process.
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China’s Process For Allowing The Export Of COVID-19 Products Without NMPA Approval
The Chinese government announced a process to export particular devices without NMPA approval.
Export Declaration Of Medical Supplies
Foreign manufacturers of COVID-19 products with FDA approval can get on China’s export white list.
Code Of Ethics Compliance Guidance Related To The COVID-19 Response
This guidance helps member companies support decision-making and mitigate compliance risks.
AdvaMedDx® COVID-19 Testing Infographic
This infographic depicts the process of COVID-19 diagnostic tests from patient sample to test results.
Listen to AdvaMed®'s Podcast
Brought to you by AdvaMed®, Medtech POV with Scott Whitaker is a podcast that covers the intersection of medtech and policy from every perspective.
ABHI – AdvaMed® Memorandum Of Understanding Regarding Cooperation And Collaboration
ABHI and AdvaMed® will coordinate activities.
VALID Act 2020 Comprehensive Summary
The VALID Act seeks to modernize FDA oversight of in vitro diagnostics.
Creating and Implementing a COVID-19 Return-to-Work Plan
The presentation slides include a decision-making framework for preparing to re-open offices.
AdvaMed® Defense Production Act Checklist / COVID-19 Trade Checklist
This short checklist provides links to relevant documents related to DPA and COVID-19 and trade in medical devices.