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EU Clinical Trial Regulations and Compliance
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36 Modules
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Live Executive Programs
Accreditation Earned: EU Clinical Trial Regulations and Compliance
This program will help you navigate EU clinical trials' regulations and provide you with skills to conduct legally compliant trials.
Key skills you will gain:
- EU Clinical Regulatory Compliance
- Clinical Trials Regulation
- Good Clinical Practice
- Clinical Trial Applications
- Informed Consent
- Clinical Trials Administration
- Pharmacovigilance
- Risk Assessment
- Ethical Research
- GDPR Compliance
- Clinical Trial Auditing
- Clinical Trial Design
- Clinical Investigations
- Safety Reporting
- Clinical Trial Insurance
- Clinical Quality Assurance (CQA)
- Clinical Trial Reporting
- EU Clinical Trials Legislation
- Clinical Trials Authorization
- Clinical Data Management
- Clinical Trial Documentation
- Investigational Medicinal Products (IMP)
- Auxiliary Medicinal Products (AxMPs)
- Data Integrity
- GCP Inspection