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eVisit

Since 2005, eVisit has been providing digital solutions tailored to the needs of the pharmaceutical industry, enhancing the quality of care and improving patient outcomes. Our success is driven by a combination of cutting-edge technology, deep medical expertise, and thorough knowledge of industry regulations. Our team of professionals ensures that our programs are compliant, effective, and aligned with the highest standards of data protection and compliance.

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Patient Support Program (PSP)

Our program is guided by internal medical advisors, who oversee its structure and ensure that it adheres to high medical standards. Their supervision guarantees effective implementation and quality service delivery. Compliance is a top priority, with dedicated teams ensuring that contracts and data protection agreements meet all legal requirements. This approach protects both patient data and institutional integrity. Regular updates, including weekly and monthly reports, are provided to healthcare partners. Notifications are sent ahead of key deadlines, and a final report at the program’s conclusion summarizes outcomes and key achievements.

Patient Support Interface (PSI)

The PSI is a specially designed system that supports healthcare professionals in monitoring the progress of patients participating in the program while ensuring patient anonymity through unique identifiers. The system does not conduct systematic data collection, and each educator only has access to their own patients’ information for the duration of the program. Sponsors do not have access to the electronic system, ensuring full confidentiality and data protection.

Market Research

In market research, expert supervision plays a crucial role in ensuring full compliance with data protection laws and regulations. Our experienced professionals oversee every stage of data collection, processing, and storage to prevent breaches and unauthorized access. By implementing robust protocols and monitoring practices, we protect sensitive data and maintain confidentiality. This approach not only reduces legal and operational risks but also enhances the credibility of research outcomes. Clients and stakeholders can trust that all information is handled responsibly and in strict alignment with privacy standards, promoting transparency and ethical practices throughout the research process.

Non-Interventional Studies

We are committed to supporting high-quality non-interventional studies through a range of specialized services. Our offerings include the development, maintenance, and continuous improvement of a proprietary electronic case report form (eCRF) system. This system is designed to streamline data collection, ensure accuracy, and maintain compliance with regulatory requirements. In addition to system management, we prioritize strict adherence to pharmacovigilance guidelines to guarantee the safety and monitoring of patients throughout the study. Our team offers comprehensive help desk support to address technical and procedural questions in real-time, ensuring smooth operations for study stakeholders. To further support the success of non-interventional studies, we provide advanced biostatistical analysis services. Our experienced statisticians perform in-depth data analyses, helping to generate robust, reliable results that meet scientific and regulatory standards. These efforts contribute to the validity and integrity of study findings, ultimately supporting evidence-based decision-making in clinical and healthcare environments.

eVisit Zrt.

Email: info@evisit.hu
Phone: +3630 637 6006
Address: 1033 Budapest, Tanuló street 1.

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002-1-1biogen
003-1-1stada
004-1-1richter
005-1-1teva
006-1-1ludbeck
007-1-1krka
008-1-1bayer
009-1-1gsk
010-1-1hartmann
011-1-1novonordisk
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022-1-1novartis
023-1-1naturprodukt
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025-1-1rivopharm
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