Examples of 'pharmacovigilance system' in a sentence
Meaning of "pharmacovigilance system"
This phrase refers to a system or process implemented by pharmaceutical companies, regulatory agencies, and healthcare professionals to monitor, detect, assess, and prevent adverse effects or any other drug-related problems after the release of a medication in the market
How to use "pharmacovigilance system" in a sentence
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pharmacovigilance system
A summary of the pharmacovigilance system master file.
Pharmacovigilance system of the marketing authorisation holder.
Reference number of pharmacovigilance system master file.
Pharmacovigilance system master file.
Structure of the pharmacovigilance system master file.
Pharmacovigilance system master file documents shall be complete and legible.
Identifier or reference number of pharmacovigilance system master file.
The pharmacovigilance system and accompanying quality management systems.
Availability and location of the pharmacovigilance system master file.
Pharmacovigilance system in albania.
Automatized pharmacovigilance system.
Quality systems should form an integral part of the pharmacovigilance system.
Content of the pharmacovigilance system master file.
Effective risk monitoring with the aid of a comprehensive pharmacovigilance system.
Implementation of a pharmacovigilance system is required to monitor the emergence of drug toxicities.
See also
Form of the documents contained in the pharmacovigilance system master file.
Union pharmacovigilance system.
Monitoring the lack of efficacy is a part of the veterinary pharmacovigilance system.
Pharmacovigilance system lp.
The document does not reflect the actual pharmacovigilance system.
The pharmacovigilance system must be strengthened through increased post marketing monitoring.
Reporting should be carried out within the existing pharmacovigilance system.
It will also establish an efficient pharmacovigilance system for medication safety in pregnancy.
Patients generally should play an increasingly active role in the pharmacovigilance system.
Sanofi has a separate pharmacovigilance system for ensuring the safety of animal health products.
Each such system shall be described in a separate pharmacovigilance system master file.
The pharmacovigilance system master file shall contain at least all of the following elements.
It coordinates inspections of veterinary pharmaceutical companies and monitors the pharmacovigilance system.
The foremost is in the pharmacovigilance system for reporting adverse side effects of medicine use.
It organises the inspection of veterinary pharmaceutical companies and the pharmacovigilance system.
Content of the Annex to the pharmacovigilance system master file.
The marketing authorisation holder shall perform a regular audit of his pharmacovigilance system.
Draft ministerial order setting up the pharmacovigilance system for traditional medicines in Burundi.
Marketing authorisation holder shall not have more than one pharmacovigilance system.
The pharmacovigilance system master file shall have an Annex containing the following documents.
The marketing authorisation holder shall be required to perform a regular audit of his pharmacovigilance system.
The EU pharmacovigilance system.
Physicians from the CeSACs were interviewed on their knowledge and usage of the pharmacovigilance system.
Put in place pharmacovigilance system, improvements to.
The marketing authorisation holder may subcontract certain activities of the pharmacovigilance system to third parties.
A summary of the applicant's pharmacovigilance system which shall include the following elements.
Only one such qualified person shall be designated for each pharmacovigilance system master file.
The pharmacovigilance system must be communicated about events threatening the patient 's safety.
A missed opportunity to genuinely strengthen the European pharmacovigilance system.
A summary of the applicant 's pharmacovigilance system which shall include the following elements,.
The sector also acts as coordinator for the EU pharmacovigilance system.
Inform about the existence of a Pharmacovigilance System dealing with drug-related adverse events.
The case of the diabetes drug Mediator highlights the weakness of the European pharmacovigilance system.
The pharmacovigilance system required in accordance with Article 72 is inadequate ;.
The MAH may subcontract certain activities of the pharmacovigilance system to third parties.
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Examples of using Pharmacovigilance
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Pharmacovigilance for medicines for veterinary use
A summary of the pharmacovigilance system master file
Pharmacovigilance responsibilities of the marketing authorisation holder
