Virtual Events Pharmacovigilance

This intensive one-day seminar will review the existing global requirements relating to pharmacovigilance in contractual agreements. The emphasis will be on practical advice as to how to remain compliant...

Join our webinar to learn about pharmacovigilance outsourcing and how an outsourced affiliate model can offer access to skilled resources with local expertise. Explore the challenges faced by marketing...

The comprehensive course offered by IPI Academy covers regulatory requirements for clinical research in Europe and the US, including the new EU Clinical Trial Regulation, CTIS, and important...

We offer a variety of training products and services that are both pre-made and customizable, addressing your technical, commercial, and personal development requirements in a comprehensive manner.

Since the introduction of the new pharmacovigilance legislation in the EU, QMS and self-audits have become an increasingly important topic. Companies have been challenged by regulators to implement risk-based...

We offer a wide selection of pre-made and customizable training products and services to meet your needs for technical, commercial, and personal development.

The course is highly interactive, with Break-Out Groups where we will examine various examples of borderline classification products and reports for market surveillance. Virtual, Eastern Standard Time...

Our offerings include a variety of off-the-shelf and customized training solutions, catering to your requirements for technical, commercial, and personal growth in a holistic manner.

Get an update of ongoing activities regarding medicines’ risk and signal management!

We offer a variety of pre-made and customized training solutions to meet your needs in technical, commercial, and personal development.

This course provides comprehensive coverage of conducting Clinical Studies in the EU, including the EU Clinical Trial Regulation, recent updates in EU-GCP, the new EU Pharmacovigilance Directive, and working...

Trusted by over 17,000 delegates across leading companies

Discover how AI and machine learning can accelerate case intake in pharmacovigilance, guaranteeing reliability and consistency. Learn about touchless case processing and its impact on patient safety. Join...

Quality Assurance, Regulatory Affairs, Clinical Research, Pharmacovigilance

This practical course provides an in-depth understanding of signal detection, signal validation & assessment as well as signal communication. The series of talks, discussions & exercises...

Trusted by over 17,000 delegates across leading companies

Regulatory Practices and promotion of trust between Health Agencies and International Organizations

Your gateway to the GCC governmental medical business

FDA Drug Topics: FDA's Postmarketing Drug Safety Surveillance System will discuss the FDA's postmarketing drug safety surveillance activities, how adverse event reports are collected and analyzed by FDA...

Postmarketing Drug Safety Compliance: Inspection Finding is a webinar that provides an overview of the PADE Compliance Program, as well as discusses inspection findings and trends from PADE inspections...

The Pharmacogenomics Behind the Investigational Treatments of COVID-19 and its High-Risk Underlying Conditions is a webinar that will provide the attendees with the opportunity to learn how to describe...

Transforming Pharmacovigilance from Operational to Scientifically-driven, in this webinar we will discuss approaches and benefits to moving from operational to scientifically-driven pharmacovigilance,...

The Business of Pharmacovigilance Understanding REMS During a Public Health Emergency takeaways the importance and value of cross-functional engagement when developing and implementing a program, such...

Scheduling and Conduct of Good Pharmacovigilance Practice Audits is intended for the pharmaceutical industry and associated service providers. It will provide pharmacovigilance and quality assurance departments...

All countries across the world are facing the same challenge: how to ensure the continued availability of medicines for the patients during the COVID-19 pandemic while maintaining high standards of medication...

This training is designed to provide participants with a foundation in regulations, FDA guidances, and risk-based principles aimed at ensuring safety of marketed drug and biological products. The training...

The presentation will illustrate how humanized preclinical animal models can advance our mechanistic understanding of IM-ADRs. This presentation will shift the focus of the session to large molecule-based...

This webinar will answer these and other questions and show risk-based approaches on how to deal with the increasing number of audits - e.g. by focusing on audits particularly in critical areas. In this...

Explore the challenges associated with managing pharmacovigilance at an affiliate level, potential solutions and explore the benefits of adopting an outsourced model. We have extensive experience in a...

Due to harmonisation of pharmacovigilance regulations and globalisation, the role of an affiliate has shifted to be a dual role – driving commercial growth along with pharmacovigilance management. At...

WB - Transforming Pharmacovigilance Workflows with AI & Automation - Discussing & debating key challenges for drug safety & pharmacovigilance professionals worldwide. Medical information call centers have...

Organizations, including pharma, med device, CROs, and medical information/poison control call centers, can leverage artificial intelligence (AI) and automation to revolutionize their end-to-end safety...

Good Pharmacovigilance is based on reliable information leading to an effective assessment of the risk-benefit balance which is crucial both in the clinical development and post-marketing safety of medicines....