12. Resources (listed in descending order of precedence)
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12. Resources (listed in descending order of precedence)
- 1 Mins to read
- DarkLight
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- National Medicinal Products Administration (NMPA) (Chinese)
- National Medicinal Products Administration (NMPA) (English)
- National Institute of Allergy and Infectious Diseases ClinRegs
- Genohub Blog – International biological material shipment information for various countries
- The Challenge of GMO Medicinal Products in Clinical Trials
- List of Contact Research Organisations in China
- IQVIA – China Embraces Decentralized Clinical Trial Solutions
- The new Good Clinical Practice 2020 in China: Views from ethical perspective
- International Research Collaboration Information Platform
- Global Regulatory Partners – Overview of Clinical Trial Application (CTA) in China
- Clinical trials handbook – Asia Pacific
- International Research Collaboration Information Platform
- Electronic Signature Law of the People’s Republic of China
- The China Personal Information Protection Law (PIPL)
- The Healthcare Law Review: China
- Operational Experiences in China and Statistical Issues on the Conduct of clinical trials during the COVID-19 Pandemic
- Remote Clinical Trials in China During the COVID-19 Pandemic
- CIRS – Medical Device Labelling Requirements in China
- Outsourcing-Pharma.com (World Courier shares its insights on successful importation of clinical trial drugs in China)
- Export2Asia – How to Get an Import Licence in China: A Complete Guide
- zhenhub The 2021 Guide to Getting Import Licence in China
- Bayer’s experience in sample exportation from China
- INCEPTUA – Navigating the Clinical Trial Supply Route in China
- Patient-Reported Outcome Measures-Challenges and Opportunities for China
- Operational Experiences in China and Statistical Issues on the Conduct of Clinical Trials during the COVID-19 Pandemic
- A review of Telemedicine in China
- Foreign Parctice for the Regulation of Wearable Devices
- The PRC Personal Information Protection Law (FINAL): A Full Translation
- China and the evolving regulatory landscape
- The Massive Guide to China Advertising Regulations
- Informed Consent and Ethical Review in Chinese Human Experimentation: Reflections on the “Golden Rice Event”
- Medicinal Product Regulation and Product Liability in China: Overview
- https://uk.practicallaw.thomsonreuters.com/4-500-8862?transitionType=Default&contextData=(sc.Default)&firstPage=true#co_anchor_a721571
- Technical Guidance for Patient-Centered Drug Clinical Trial Design (English Translation)
- Technical Guidelines for Patient Centered Drug Benefit-Risk Assessment (Trial) (English Translation)
- Technical Guiding Principles for the Implementation of Patient-Centered Drug Clinical Trials (English Translation)
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