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Let Regulations Work for You!

How do you strengthen a system which complies both with regulatory and industry standards? Our team of senior pharmacovigilance experts will show you how to construct functional systems with ingenuity.

About us


Pharmacovigilance Training

The competence of your pharmacovigilance team members is related to your audit and inspection results. To make sure our clients are prepared, we provide all levels of pharmacovigilance training and courses can be customized to meet specific requests.

  • Extensive PV Training for different groups
  • Tailored PV Training on concrete topics
  • Customized training on EU GVP
QPPV Office Services

Review of existing pharmacovigilance processes can make way for positive changes with dramatic increases in efficiency.


Signal Management

Risk Management

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Signal and Risk Management

Local and regional regulatory authorities are constantly updating safety information which requires reference safety data and labeling to be updated. This is time-consuming for a QPPV. iVigee has created a monitoring solution that performs these tasks.

Quality Assurance

Label Monitoring Updates

PV Network

Compliance


Local and regional regulatory authorities are constantly

Jana Hyankova chairing International QA Conference

Our PV team has been busy this spring!

20.05.2024

Jan Petracek speaking at EUFEPS Annual Meeting 2024

Pharmacovigilance Transformation...find out what is changing and what will stay at the 2024 European Federation for Pharmaceutical Sciences (EUFEPS) annual meeting.

15.05.2024

New starter: Lucia Matejkinova

We're thrilled to announce that Lucia Matejkinova joined iVigee as our new QPPV Office Lead on March 1, 2024! She oversees the management of our QPPV office and serves as the EU QPPV for our clients.

09.05.2024

Quality management system

The QMS is fundamental to all aspects of pharmacovigilance. In addition to building your QMS, we can provide full Quality Management System reviews. If your organization has recently finished an inspection or audit, our QMS services focus on corrective and preventative actions (CAPA) to meet any and all findings from audits or inspections. CAPA(s) are provided, with follow-up until positive corrections are documented and completed.

Standard Operating Procedures

Standard Operating Procedures (SOP) describe the critical processes within your pharmacovigilance system. At iVigee, we may review your existing SOPs, develop new SOPs, or perform a batch review for multiple/all SOPs in place impacted by new regulations.


Comparing your PV system to industry standards

The QMS is fundamental to all aspects of pharmacovigilance. In addition to building your QMS, we can provide full Quality Management System reviews. If your organization has recently finished an inspection or audit, our QMS services focus on corrective and preventative actions (CAPA) to meet any and all findings from audits or inspections. CAPA(s) are provided, with follow-up until positive corrections are documented and completed.

AI Technology Pharmacovigilance
The safe way through Pharmacovigilance

Rest assured knowing your current and future pharmacovigilance systems are meeting your regulatory, fiscal, and operational requirements

Future versions of iViReg will showcaseWorld leading technology company that specialises in combining
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  • The FDA's discussion paper, particularly in its Post-market Surveillance section

    This year marked significant strides in AI, with leading regulatory bodies inviting public commentary on their perspectives regarding AI and Machine Learning (AI/ML) in drug development. While the FDA's consultation period concluded earlier in August (find the paper here), the EMA's window remains open until year-end.

  • At iVigee, we are fully committed

    Leveraging the latest AI advancements for our clients' benefit. We have thoroughly reviewed both papers and have submitted our comments, contributing to shaping the future of AI in pharmaceuticals.

  • Are you an innovator or early-adopter looking to enhance

    Replace existing predictive ML-based pipelines with the realities and power of Generative AI? Seize the opportunity to innovate and transform your pharmacovigilance strategies with our cutting-edge Expert AI Implementations.

  • The course is designed to give a comprehensive understanding

    iVigee is a world-leading technology company that specialises in combining AI, IT, and industry expertise to create simple, powerful, and elegant solutions that revolutionize the field of pharmacovigilance.

Marcela is an experienced PV professional with extensive expertise in the setup, use and management of Pharmacovigilance System Master Files (PSMFs) and is sharing her knowledge and best practices about how to practically manage your own PSMFs.

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Jan Petracek speaking at EUFEPS Annual Meeting 2024

Pharmacovigilance Transformation...find out what is changing and what will stay at the 2024 European Federation for Pharmaceutical Sciences (EUFEPS) annual meeting.

15.05.2024

New starter: Lucia Matejkinova

We're thrilled to announce that Lucia Matejkinova joined iVigee as our new QPPV Office Lead on March 1, 2024! She oversees the management of our QPPV office and serves as the EU QPPV for our clients.

09.05.2024

April Regulatory Intelligence News!

Are you aware of the recent update from Swissmedic?

07.05.2024

The results are in!

We asked about the maturity of your regulatory intelligence process

06.05.2024

67th EPSA General Assembly

🌍 Exciting News! We're participating in the upcoming 67th EPSA (European Pharmaceutical Students’ Association) General Assembly today in Prague.

02.05.2024

Pharmacovigilance Regulatory Intelligence Process

How mature is your regulatory intelligence process? 📶

01.05.2024

We are proud to be exhibiting at booth D5 at this year’s DIA Europe conference in Brussels from the 12th to the 14th of March. And we’ll be demonstrating our thought leadership from the top with CEO Jan Petracek co-chairing the Wednesday 13th track 07 Pharmacovigilance and Safety session - How to build a sustainable Pharmacovigilance Ecosystem?

Global Regulatory Intelligence platform
90+ countries, fully validated

Generative AI can be deployed in various processes such as monitoring data sources and case intake, managing safety signals and risks, analysing complex data, reporting adverse events, improving submissions and compliance, and providing training, education, and patient support.

By making Generative AI and LLM technologies central to our strategy, we ensure that your business is not only keeping pace but also setting the standard for AI-driven pharmacovigilance solutions. The AI revolution at the enterprise level necessitates a cultural shift, and we recognize that the newly introduced business processes, more robust infrastructure, real data readiness, and having the right talent all require a well-considered change-management approach.

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