Nowadays when medicine and pharmacology are developing rapidly it is necessary to have a standardized approach to classify medical terms. MedDRA (Medical Dictionary for Regulatory Activities) is such a standard. In this article, we will look at the main reasons why the use of MedDRA is mandatory for everyone involved in the medical industry
- Communication facilitation
One of the main goals of MedDRA is to ensure the accuracy and completeness of information about medicines. Thanks to the use of a standardized terminology, specialists from different countries and cultures can easily exchange information and understand each other. This helps to avoid misunderstandings and mistakes that may lead to negative consequences for patients.
- Accuracy and Completeness of Information
MedDRA contains more than 100,000 terms related to drugs, diseases, and treatments. The use of this vocabulary allows medical professionals to provide accurate and complete information about the patient's condition, which contributes to the correct choice of treatment and increases its effectiveness.
- Reducing the risk of errors
Errors in medical data can lead to serious consequences for patients. Using MedDRA helps to avoid such mistakes, as all terms in the dictionary are carefully checked and approved by medical and pharmacology experts. This ensures the reliability and validity of the information provided to patients and healthcare professionals.
- Fast Track for New Medicines
When submitting for a marketing authorization of new medicines, it is necessary to provide a lot of information about the drug, including its composition, indications, side effects, etc. Using MedDRA allows this information to be collected and processed quickly and accurately, which reduces time required to complete all the necessary procedures.
- Improving the Quality of Clinical Trials
Clinical trials are one of the key stages in the development of new medicines. They allow to assess the efficacy and safety of a drug before it is released to the market. The use of MedDRA in clinical trials provides uniformity and accuracy in data collection and analysis, which improves the quality of research results and contributes to informed decision-making.
Thus, MedDRA is a good tool for all participants in the medical industry. Its use improves communication, ensures the accuracy and completeness of information, reduces the risk of errors and misunderstandings, speeds up the process of registration and approval of new medicines, and improves the quality of clinical trials and their results. Therefore, the introduction of MedDRA into everyday practice is a prerequisite for the successful development of medicine and pharmacology in the future. If you are not yet familiar with this dictionary, then our company may help you with its application.
