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NON-INTERVENTIONAL STUDIES
Conducted to gather information on the safety and tolerability of a medicinal product.
SERVICES INCLUDE
Development of medical documents
Identification of clinical sites (clinics) and organization of the investigator team's work
Organization of document review by an Independent Ethics Committee
Project management
Data statistics and evaluation
Writing of the final report
Writing of publications
SERVICES INCLUDE
STAGES OF NON-INTERVENTIONAL STUDIES
We always operate in compliance with current legislation on medicinal product regulation
We will calculate the final cost and procedure timelines based on your request
What is a non-interventional study?
A non-interventional study is a clinical study that differs in its algorithm from a classical clinical trial. In its implementation, data on the efficacy and safety of a medical product are collected through routine observation of events without active intervention.
PharmAssistance LLC has many years of experience in conducting non-interventional studies aimed at collecting and analyzing data that help improve the quality of medical care and ensure patient safety. We work in accordance with current legislation in the field of drug distribution.
The essence of non-interventional studies
Non-interventional studies in medicine are mostly observational and post-marketing studies of medicine safety. They offer many benefits to both researchers and patients:
- Gathering information from real-world practice provides a better understanding of how medicines work in different populations.
- Research helps identify potential risks and side effects early on
- NRI results help physicians and patients make more informed treatment decisions.
Non-interventional research with the help of PharmAssistance
We offer a full range of services to organize and conduct NRIs, including
- Study design – developing protocols that meet international standards and regulatory requirements.
- Research site identification.
- Organization of research studies and support during their execution.
- Analyzing results using statistical methods to identify key trends and patterns.
- Writing a detailed final report that can be used for further research and to inform the medical community and regulatory agencies.
Why choose us?
- Our team consists of highly qualified specialists with many years of experience in clinical trials and pharmacovigilance.
- We develop customized solutions to meet the needs of our clients.
- We use the latest tools and platforms for data collection and analysis to ensure high accuracy and reliability of results.
How to contact us?
If you are interested in conducting a non-interventional study or would like to learn more about our services, please contact us. Our team is ready to answer all your questions and assist you at every stage of the study.
