NeuAge Institute (NAI)

3 Career Paths You Can Pursue After Earning Your Pharmaceutical Regulations Certificate

pharmaceutical industry training
Pharmaceutical regulations are crucial to the release of new drugs, biologics, medical devices, and combination products. Those working in the field of regulatory affairs will find their expertise is needed across different companies and at different stages of their product development. From testing and manufacturing to marketing and distribution, regulatory standards are applied to promote the safe and effective release of pharmaceutical products on the market.  

Students in the Regulatory Affairs program at NeuAge Institute will develop a good understanding of regulatory frameworks, compliance requirements, and Good Manufacturing Practices. If you’re interested in learning where your expertise can take you, read on for a look at the career paths open to Regulatory Affairs professionals. 

Become a Regulatory Affairs Specialist 

A regulatory affairs specialist is responsible for ensuring that a pharmaceutical company is meeting the regulatory standards that apply to their products. This includes industrial, local, federal, and global regulations. Often, you’ll be liaising with regulatory or government bodies to gain a clear understanding of current protocols. It’ll then be your job to communicate the relevant policies to pharmaceutical companies and update them on any regulatory changes that could impact their practices. 

Strong attention to detail and a keen awareness of regulatory pathways are essential to success in this role. After all, you’ll have to stay on top of the requirements surrounding the market to promote the safe and effective release of new products. That means having a clear understanding of a company’s specific products, as well as the broader sector in which that company operates. 

Students earning their pharmaceutical regulations certificate at NeuAge Institute will study the regulatory pathways for drugs, biologics, medical devices, combination products, and dietary supplements. Along with courses in Canadian, European, and International regulatory submissions, you’ll be ready to apply your knowledge as a regulatory affairs specialist. 

pharmaceutical regulations certificate
Act as a point of contact between pharmaceutical companies and regulatory bodies

Work as a Compliance Specialist After Pharmaceutical Industry Training

As regulatory standards continue to evolve, compliance specialists are needed to help pharmaceutical companies navigate the regulations that apply to them. In other words, they interpret regulatory requirements for organizations and ensure they are acting in compliance with them.

As a compliance specialist, you’ll oversee a pharmaceutical company’s products, practices, and facilities to verify compliance on all levels. Regulatory departments are stringent and pharmaceutical companies will need to perfect their practices to ensure the legality of their business. In some cases, you’ll have to identify areas of improvement and recommend a plan for companies to strengthen their compliance. In that sense, risk management is one of the key duties of a compliance specialist. 

During pharmaceutical industry training, students will explore courses in Pharmacovigilance and Risk Management as they work towards their Regulatory Affairs Certification (RAC) Drug Exam. By encouraging pharmaceutical companies to develop foolproof business practices, you can help them to streamline their operations on every level. 

pharmaceutical careers
Help companies develop compliant strategies with a pharmaceutical regulations certificate

Apply Your Skills as a Clinical Research Associate

If you’re looking to apply your knowledge of regulatory affairs to the clinical trial stage of new products, then consider becoming a clinical research associate. A clinical research associate is responsible for overseeing clinical trials and ensuring that study protocols are being followed. This involves examining study data and performing quality assurance audits. In this role, you’ll need to demonstrate a clear understanding of regulatory requirements that apply to the clinical stage of pharmaceutical products. 

With courses in Good Clinical Practices (GCPs), students in the regulatory affairs program at NeuAge Institute will learn about the different phases of clinical trials for drugs, biologics, and medical devices, along with the monitoring and auditing process. Through an applied and practical approach to your training, you’ll be ready to take your expertise to pharmaceutical companies, hospital research departments, or clinical contract agencies. 

Are you interested in learning more about pharmaceutical careers open to our graduates?

Contact NeuAge Institute today.

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