InnoVigilance Academy

12/30/2023

🌟 Nous avons le plaisir d'annoncer la reprise de notre série d'ateliers de l’InnoVigilance International Academy™ pour 2024, mettant l'accent sur la pharmacovigilance et la sécurité du médicament! 🤝 Après le succès de nos formations en ligne et en présentiel, nous sommes ravis de continuer à partager notre expertise. 🚀 Soyez prêts à vous immerger dans une expérience d'apprentissage inégalée. Restez à l'affût pour plus de détails!
Prochaine session: Alger 18-19 février 2024. "

Lien de pré-inscription : https://docs.google.com/forms/d/e/1FAIpQLSfH0LNSBjcAITMHjuZ3skeOSrK2X7Jm98Vkd3DqG0xke-52Mg/viewform (nombre de places limitées à 20)

09/27/2022

Congratulations Dr. Omar AIMER and best of luck for your new responsibilities at the International Society of Pharmacovigilance (ISoP Online)

05/28/2022

05/12/2022

Voulez-vous acquérir les fondements et standards internationaux en pharmacovigilance et sécurité des médicaments qui vous permettront d’exceller dans ce domaine et vous ouvriront les portes de l’industrie pharmaceutique et de l’évolution dans votre carrière?

InnoVigilance International Academy™ leader en formation dans le domaine entame sa série d’ateliers/workshops en présentiel dans un bon nombre de métropoles et capitales mondiales: Alger, Paris, Toronto, Boston, Chicago, San Francisco et bien d’autres.

Alger : 17 et 18 Juillet 2022

Jour 1
Matin: Bases de pharmacovigilance
Après-midi - Réglementation (ICH, FDA, EMA, Santé Canada et CNPM)

Jour 2
Matin : Opérations (traitement des cas, causalité, qualité, codage MedDra et pratique sur bases de données)

Après-midi - Rapports périodiques Détection du signal et Gestion de risque.

Pour plus d’informations sur les dates, lieu, inscriptions et tarifs veuillez nous contacter par e-mail: info@innovigilance.com , page Facebook et page LinkedIn.

Vite! Le nombre de places est limité.

09/29/2021

Do you know the FDA sections?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

09/27/2021

What is the finding of the clinical trial?

Do you like to be a certified professional in pharmacovigilance and drug safety?
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09/25/2021

Standard Operation Procedures are the quality control documents which implement company policy to ensure regulatory obligations are fulfilled, personnel are trained, and tasks are accurately documented.
Work Instructions documents are then derived from the SOPs to provide detailed guidance to staff in the ex*****on of the tasks outlined in the SOPs.
The implementation of SOPs is audited, inspected, and regulated by the regulatory authorities. SOPs are therefore a pivotal component of the Drug Safety system, the main challenge of Pharmacovigilance Drug Safety teams is that they should be accurate and maintained continuously.

That’s what we will discuss in our monthly webinar with our Expert guest.

See you then!

09/22/2021

What are the scops that MEDDRA covers?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

09/20/2021

Have you ever heard about Orphan Medicines?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

09/19/2021

Standard Operation Procedures are the quality control documents which implement company policy to ensure regulatory obligations are fulfilled, personnel are trained, and tasks are accurately documented.
Work Instructions documents are then derived from the SOPs to provide detailed guidance to staff in the ex*****on of the tasks outlined in the SOPs.
The implementation of SOPs is audited, inspected, and regulated by the regulatory authorities. SOPs are therefore a pivotal component of the Drug Safety system, the main challenge of Pharmacovigilance Drug Safety teams is that they should be accurate and maintained continuously.

That’s what we will discuss in our monthly webinar with our Expert guest.

See you then!

09/15/2021

How to ensure the validity of the report in PV?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

09/13/2021

What are the important steps that we used to manage the signal?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

09/08/2021

What are the components of the pharmacovigilance system?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

09/06/2021

What are the steps that need to record an ADR report?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

09/01/2021

What are the three principles that are important in health research?

Do you like to be a certified professional in pharmacovigilance and drug safety?
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08/30/2021

What are the steps that use to placing drugs in the EU market?

Do you like to be a certified professional in pharmacovigilance and drug safety?
Join us now!

08/29/2021

“Quality” is one of the key areas in drug safety and pharmacovigilance (PV). It consists of quality planning, quality control, quality assurance and quality improvements which are crucial for ensuring correct analysis and undertaking corrective actions in a timely manner and helps to safeguard the health of the patients and allows safe use of the drug.

Both FDA and EMA (and other agencies) have made it clear that they expect the quality to be built into drug safety (and all pharmaceutical systems) by releasing guidance and good practices.

Hence, in each PV unit a quality management system must be implemented including a quality policy, approved standard operating procedures (SOPs), quality control (QC) procedures, key performance indicators (KPI), jobs description and training plans should be in place covering the entire PV process. This quality management system has to ensure that all PV activities are conducted in conformity with the highest ethical standards and relevant regulatory requirements and contractual obligations to any partners.

That’s what we will discuss in our monthly webinar with our Expert guest. See you then!