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New Directions in Pharmacovigilance Date: Thursday, September 10, 2015, Time: 8:30 am 5:15 pm Location: Alumni Hall, Alex Greek Room, 157 S raphin-Marion, University of Ottawa This one-day workshop
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How to fill out new directions in pharmacovigilance
How to fill out new directions in pharmacovigilance:
01
Familiarize yourself with the new guidelines and directions provided by the regulatory authorities in your country or region.
02
Review the objectives and scope of the new directions to understand the changes and requirements in pharmacovigilance practices.
03
Ensure you have access to the necessary resources, including updated forms, databases, and reporting systems, to comply with the new directions.
04
Train your pharmacovigilance team on the changes introduced by the new directions and provide them with the necessary guidance and tools to implement them effectively.
05
Follow the specific instructions outlined in the new directions when collecting, assessing, and reporting adverse drug reactions.
06
Keep accurate and detailed records of all pharmacovigilance activities carried out in accordance with the new directions.
07
Regularly monitor and evaluate the effectiveness of your pharmacovigilance practices to ensure compliance with the new directions and identify areas for improvement.
08
Stay updated with any updates or revisions to the new directions and adapt your pharmacovigilance processes accordingly.
Who needs new directions in pharmacovigilance:
01
Regulatory authorities responsible for overseeing drug safety and efficacy.
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Pharmaceutical companies and manufacturers.
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Healthcare professionals, including physicians, pharmacists, and nurses, involved in prescribing, dispensing, or administering medications.
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Clinical researchers conducting clinical trials.
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Consumers and patients who may experience adverse drug reactions or have concerns about medication safety.
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Pharmacovigilance professionals and experts responsible for monitoring and ensuring drug safety in healthcare settings.
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