NeuAge Institute (NAI)

3 Trends Students in Pharmacovigilance Courses Should Know

Drug safety and regulation practices are continually evolving to meet the current demands of public health. This is more true than ever since the onset of the COVID-19 pandemic. The pandemic brought various challenges to pharmacovigilance due to the limited availability of clinical resources and researchers during this period. 

At the same time, the decline in clinical trials opened opportunities to set new standards and more effective safety practices around drug development. It highlighted the relevance of proper pharmacovigilance in public health emergencies and urged researchers to adapt methodologies to ensure future growth. With this in mind, here’s a look at how some of these ideas have shaped new trends in pharmacovigilance.  

1. Automating Data Collection

The availability of healthcare data has vastly improved in recent years, thanks to new technologies that make collecting patient data easier than ever. This kind of data is highly valuable in providing evidence on drug reactions that can improve drug safety assessments. But accuracy and efficiency in the data collection process are essential to make the most of these resources.

Automation offers numerous benefits to pharmacovigilance practices when it comes to managing a lot of data. Automation helps to eliminate human error, save time, and decrease expenses. After your pharmaceutical industry training, look out for technologies like Electronic Data Capture that can transform the way data is collected and evaluated to speed up clinical trials and enhance pharmacovigilance success.

pharmacovigilance courses
Automation is improving practices for those with pharmaceutical industry training

2. Adapting to Public Health Emergencies 

The quick onset of COVID-19 caused an urgent demand to accelerate the approval of drugs and vaccines. In the absence of treatment for COVID-19, health care professionals sought to repurpose drugs already approved for other conditions. 

These events highlighted the need to quickly supply data on drug safety in a post-marketing setting to identify any risks to patients. At the same time, there is now greater awareness of the importance of risk communication to healthcare providers and patients. This ensures that both parties can make informed decisions about the use of new drugs and vaccines. 

Students earning their pharmacovigilance certificate at the NeuAge Institute will be well-equipped for this reality with knowledge of the practical aspects of drug safety reporting during clinical trials and in the pre and post-approval periods. 

pharmaceutical industry training
Risk communication is more important than ever after COVID-19

3. Changes to the Workplace for Those With Pharmacovigilance Certification 

2022 is seeing a big emphasis on collaboration and integration across different healthcare sectors. Pharmaceutical teams understand the value of working more closely together, especially across the different areas and stages of drug development. Communication and data are passing freely, and business processes are becoming more streamlined. At the same time, you can expect to see a bigger shift to remote work and the need for better coordination to manage workloads across different teams. 

Students at NAI will learn Good Clinical Practices (GCP), the regulatory framework of drug development, and the organization and management of studies conducted across multiple phases to assess the safety and effectiveness of drugs. With specialized knowledge in the field, you’ll be ready to meet the demands of the workplace and collaborate with other specialists in the pharmaceutical sector. 

Are you interested in pharmacovigilance courses?

Contact the NeuAge Institute to get started.  

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