NeuAge Institute (NAI)

Identify the Challenges of Pharmacovigilance on a Global Scale During Pharmacovigilance Courses

Pharmacovigilance is an important field that serves to protect the public from the adverse effects of medical drugs. Here, industry experts thoroughly analyze and assess different licensed drugs in order to identify any unreported negative side effects. However, as the world becomes increasingly globalized and new technology gets introduced, the pharmaceutical industry is encountering new trends that can cause challenges within the pharmacovigilance field.

At the NeuAge Institute, students completing their pharmacovigilance training have an opportunity to study drug development. As such, they are able to develop a broader perspective of the industry, uncovering objectives and challenges on a global scale. Despite the exciting new developments coming ahead, the industry has yet to overcome some of its key issues. Across the world, the industry experiences many similar challenges. Read on to discover what those may be and develop a more in-depth view of the global pharmacovigilance industry!

Enhancing Communications with the Public

Relying on detailed reports by practitioners is one of the most essential ways to gather information on the adverse effects of a medical drug. However, industry professionals need to develop more effective ways to communicate with patients and encourage them to be more actively involved. While this may not be a new challenge, it’s one that can prevent industry experts from gathering even more valuable information.

Reports created by patients can serve as additional resources that complement other documents provided by healthcare providers. However, the quality of these reports must be vetted to determine their impact and usefulness. Here, ensuring that the right resources are spent on the right efforts is another part of the challenge. As such, students in pharmacovigilance courses may be keen to know that enhancing communications between pharmacovigilance experts, patients, practitioners, and other key stakeholders is a key step to improving the industry.

pharmacovigilance and drug safety training
Providing patients with useful information about medical drugs after pharmacovigilance courses is part of improving communication in the field

Standardizing a Globalized Approach to Pharmacovigilance

It should be noted that pharmacovigilance systems differ around the globe. In the US, practitioners and patients typically report unwanted side effects of medical drugs directly to the pharmaceutical manufacturers, who may then report back to the FDA. In other places around the world, regional pharmacovigilance centers collect drug reports and send them over to the national centers. These different procedures can make it difficult for the industry to develop a standardized approach on a global scale.

It has been suggested that establishing a set of international best practices within the pharmacovigilance field may help bridge these differences. However, the process of doing so will likely face numerous challenges, especially since the delivery of healthcare and the development stages of drug regulatory and pharmacovigilance systems differ around the world. Students completing their pharmacovigilance and drug safety training may benefit from keeping this challenge in mind as they progress forward into their studies.

pharmacovigilance certification
Developing best practices in pharmacovigilance can be one way to overcome global challenges in the field

Using Data and Technology Efficiently after Pharmacovigilance Courses

It comes as no surprise that technological advancements and data analytics can significantly help the field of pharmacovigilance. However, it’s important for this data to provide notable value. As a result, pharmacovigilance experts must seek new ways to maximize the impact and utility of the data they generate.

This challenge can also apply to the minimal data on product identifiers. Without uniform data, pharmacovigilance systems may continue to be out of sync with product quality systems, making data less productive than it could be. By reviewing the use of data in the field, and developing new ways to leverage technology, industry experts can continue to enhance pharmacovigilance systems for a better impact in the future.

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