Impacts of PV on Covid-19
The current challenges posed by the COVID-19 pandemic have also prompted regulatory agencies to reconsider their requirements and have emphasised the importance of electronic reporting to ensure data exchange for patient safety. A strong process for regulatory intelligence maintenance, a rapid change-implementation process and robust system to enter rule-based decisions can contribute to ensure compliance and quality.
- Digital Disruption
- Patient Centricity
- Transforming Trials
Related Conference of Impacts of PV on Covid-19
November 25-26, 2025
4th World Congress on Medicinal Chemistry and Computer Aided Drug Design
Paris, France
November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
Zurich, Switzerland
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3rd International Conference on Current Advances In Pharmaceutical Industry And development
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23rd International Pharmaceutical Sciences & Life Saving Drugs
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11th International Conference on Future Pharma and Innovations
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8th International Conference and Exhibition on Pharmaceutical Development and Technology
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26th World Congress on Pharmaceutical Sciences and Innovations in Pharma Industry
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19th International Conference and Exhibition on Pharmacovigilance & Drug Safety
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32nd International Conference on Advanced Clinical Research and Clinical Trials
London, UK
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Impacts of PV on Covid-19 Conference Speakers
Recommended Sessions
- Adverse drug reactions
- Artificial Intelligence in Signal Detection
- Drug Development
- Drug Safety
- Drug Tolerance
- Good Pharmacovigilance Practices
- Impacts of PV on Covid-19
- Market Research Programs
- Patient Support Programs
- Pharmaceutical Toxicology
- Pharmacokinetics and pharmacodynamics
- Pharmacovigilance
- Pharmacovigilance Operations
- Pharmacovigilance risk management plans
- PV Inspection and Audit Readiness
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