Starting a new career in a different country is no small feat. But for medical writer Terissa Barnes, it was a challenge worth taking on. A 2022 graduate of the Quality Assurance and Regulatory Affairs (QARA) program at AAPS, Terissa leveraged her education and determination to build a rewarding career in the pharmaceutical industry. Today, she thrives at Cliantha Research Limited, where her passion for science and communication align seamlessly. Bridging Academia and the Pharmaceutical Industry Originally from Jamaica, Terissa’s professional journey began as a scientist in academia. But her move to Canada signaled the start of a new chapter… READ MORE »
As the pharmaceutical industry grows, ensuring product safety and quality has never been more crucial. One key component of this process is Cleaning Validation, a practice designed to prevent cross-contamination between pharmaceutical batches. To help professionals excel in this essential area, AAPS is offering a new comprehensive Cleaning Validation Workshop scheduled for October 17, 2024. This workshop will give participants a robust understanding of Cleaning Validation procedures, regulatory compliance, and hands-on experience in a GMP laboratory setting. Let’s explore what this exciting workshop offers and why it’s a must-attend event for professionals in Quality Control (QC) and laboratory operations. What.. READ MORE »
Quality Assurance training is crucial for preparing GMP audits and ensuring compliance with stringent regulatory standards in the pharmaceutical industry. These audits, though daunting, can become opportunities to strengthen your processes, systems, and product quality with the proper preparation and strategies. Below, we outline some best practices for preparing for GMP audits and achieving consistent, successful outcomes. Understand Regulatory Requirements With Our Comprehensive Quality Assurance Training The first step in preparing for a GMP audit is understanding the relevant regulatory requirements. Since GMP guidelines and regulations vary by region and market, staying informed about guidelines specific to your product type.. READ MORE »
Maintaining the integrity of pharmaceutical products is paramount in the pharmaceutical quality assurance (QA) training industry. One essential component of QA in pharmaceutical training is compliant temperature mapping. This process ensures that pharmaceutical products are stored and transported within their designated temperature ranges, preserving their efficacy and safety. Understanding temperature mapping is crucial for QA professionals. AAPS’s upcoming workshop can provide invaluable insights into this vital area. Why Temperature Mapping Matters in Pharma QA Training Temperature is a critical factor in the storage and transportation of pharmaceutical products. Each medication has specific storage requirements, including the optimal temperature, outlined on.. READ MORE »
