What is the regulatory process in Canada and how are patients’ safety matters handled in clinical trials?
In Canada, clinical trials are regulated by Health Canada, the federal department responsible for overseeing the safety, efficacy, and quality of health products. The regulatory process and patient safety matters in clinical trials are handled through a comprehensive framework that emphasizes ethical considerations and participant protection. Let's explore the regulatory
Why should I participate in clinical trials?
Deciding to participate in a clinical trial is a personal choice that should be carefully considered. Here are some factors to keep in mind when deciding whether to participate in a clinical trial: Understand the Purpose: Educate yourself about the specific clinical trial you are considering. Understand its objectives, the
What are the different phases of clinical trials
Phase 1: These trials involve a small number of healthy volunteers and focus on assessing the safety, dosage, and potential side effects of the intervention. The primary goal is to determine the drug's appropriate dosage range. Phase 2: In this phase, the trial is expanded to include a larger
The Role of Clinical Trials in Drug Development
The development of new drugs is a complex and rigorous process that demands extensive research, testing, and evaluation before they can be deemed safe and effective for public use. One of the critical stages in this process is clinical trials. These trials, conducted with human participants, are the cornerstone
What are Clinical Trials (CTs)?
Clinical Trials are research studies conducted to evaluate the safety, efficacy, and side effects of new drugs, medical devices, treatments, or interventions in human participants. These trials are designed to gather scientific data and evidence to determine whether a particular intervention is effective in preventing, diagnosing, or treating a specific
