official trial

简明释义

正式试航

英英释义

例句

1.The new drug will undergo an official trial 官方试验 before it can be approved for public use.

新药将在获得公众使用批准之前进行一次official trial 官方试验。

2.Participants in the official trial 官方试验 were carefully selected based on their medical history.

参与official trial 官方试验的人员是根据他们的病史仔细挑选的。

3.Before launching the product, the company conducted an official trial 官方试验 to ensure safety and efficacy.

在推出产品之前，公司进行了official trial 官方试验以确保安全性和有效性。

4.The results from the official trial 官方试验 will be published in a peer-reviewed journal.

来自official trial 官方试验的结果将发表在同行评审的期刊上。

5.During the official trial 官方试验, researchers will collect data to evaluate the effectiveness of the treatment.

在official trial 官方试验期间，研究人员将收集数据以评估治疗的有效性。

作文

In the field of medical research, the term official trial refers to a structured process where new treatments or drugs are tested on human subjects to evaluate their effectiveness and safety. This process is crucial for ensuring that any new medical intervention is both safe and beneficial before it is made available to the public. An official trial typically involves several phases, each designed to answer specific research questions and gather comprehensive data. The first phase, known as Phase I, usually involves a small group of healthy volunteers. The primary goal here is to assess the safety of the drug, determine appropriate dosage levels, and identify any potential side effects. This phase is critical because it sets the foundation for the subsequent phases of the official trial. If the drug passes this initial test, it moves on to Phase II, where it is administered to a larger group of patients who have the condition that the drug is intended to treat. This phase focuses on assessing the drug's effectiveness and further evaluating its safety.Phase III is often considered the most important step in the official trial process. During this phase, the drug is tested on thousands of patients across multiple locations to confirm its effectiveness, monitor side effects, and compare it with standard treatments. The results from Phase III trials are critical as they provide the evidence needed for regulatory bodies, like the Food and Drug Administration (FDA) in the United States, to approve the drug for public use.Following successful completion of these phases, the data collected is submitted for review, and if approved, the drug can be marketed to the public. However, even after a drug is released, ongoing monitoring continues to ensure long-term safety and efficacy. This post-marketing surveillance is an essential part of the official trial process, as it helps identify any rare side effects that may not have been apparent during the initial trials.The importance of official trials cannot be overstated. They are fundamental in advancing medical science and improving patient care. Without rigorous testing through official trials, there would be no way to guarantee that new treatments are safe and effective. Moreover, official trials contribute to building public trust in the healthcare system, as patients can feel more confident knowing that treatments have undergone extensive evaluation before reaching the market.In conclusion, the concept of official trial is vital to the development of new medical therapies. It ensures that any new drug or treatment is thoroughly tested for safety and efficacy, protecting the health and well-being of patients. As we continue to advance in medical research, the role of official trials will remain pivotal in shaping the future of healthcare and improving outcomes for patients worldwide.

在医学研究领域，术语官方试验指的是一个结构化的过程，在这个过程中，新治疗方法或药物在人体上进行测试，以评估其有效性和安全性。这个过程对于确保任何新的医疗干预在向公众提供之前是安全且有益的至关重要。官方试验通常涉及几个阶段，每个阶段旨在回答特定的研究问题并收集全面的数据。第一阶段，称为第一期，通常涉及一小组健康志愿者。这里的主要目标是评估药物的安全性，确定适当的剂量水平，并识别任何潜在的副作用。这个阶段至关重要，因为它为官方试验的后续阶段奠定了基础。如果药物通过了这一初步测试，它将进入第二期，在这一阶段，药物被给予一组更大的患者，这些患者具有药物旨在治疗的疾病。这个阶段着重于评估药物的有效性并进一步评估其安全性。第三期通常被认为是官方试验过程中的最重要步骤。在这一阶段，药物在多个地点对成千上万的患者进行测试，以确认其有效性，监测副作用，并与标准治疗进行比较。第三期试验的结果至关重要，因为它们提供了监管机构（如美国食品药品监督管理局FDA）批准药物上市所需的证据。在成功完成这些阶段后，收集的数据会提交审核，如果获得批准，药物就可以向公众销售。然而，即使药物发布后，持续监测仍然在进行，以确保长期的安全性和有效性。这种上市后监测是官方试验过程的重要组成部分，因为它有助于识别在初始试验中可能未显现的稀有副作用。官方试验的重要性不容低估。它们对推动医学科学和改善患者护理至关重要。如果没有通过官方试验进行严格测试，就无法保证新治疗方法的安全性和有效性。此外，官方试验有助于建立公众对医疗系统的信任，因为患者可以更有信心地知道，治疗方法在进入市场之前经过了广泛的评估。总之，官方试验的概念对新医疗疗法的发展至关重要。它确保任何新的药物或治疗方法在安全性和有效性方面经过彻底测试，从而保护患者的健康和福祉。随着我们在医学研究中的不断进步，官方试验的角色将继续在塑造医疗保健的未来和改善全球患者的结果中发挥关键作用。