Understand how new therapies are tested for efficacy, safety, and monitored post-trial, the constant process of evaluating result with other countries involved in proving a new treatment or drug’s safety for patient use.
Find out more on enhancements to the trial search, clinical data management and analysis that shall strengthen the clinical trials process as well as the outcome of the patients.
This blog covers their advantages, the procedure for approval, and why they matter in terms of saving money and increasing the number of patients who can benefit from medications that involve biologics.
How monitoring facilitates achievement of patient safety promotion, establishment of public confidence and drug advancements.
Find out how clinical trials being conducted in developing countries are changing the facet of global medical research.
Learn how inexpensive services, a demographically diverse patient pool, and a well-developed healthcare industry make India a favorable environment for clinical research.
Find out more about the ongoing developments, issues and marked progress influencing development of these vital areas of medicine.
There are most often a lengthy and comprehensive process of approval for a particular drug which has to pass several phases of clinical trials and further regulatory assessments of safety.
Explore the role of placebos in clinical trials, including their impact on measuring treatment efficacy and the ethical challenges they present.
Identify the responsibilities of IEC, ERB and REB in clinical trials.
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