Are you considering advancing your pharmaceutical career but need help fitting education into your busy schedule? At AAPS, our pharma courses online are specifically designed to help you grow and succeed in today’s competitive pharmaceutical industry. Here’s why 2025 is the perfect year to plunge into online pharmaceutical education. 1. Flexible Learning That Works for You One of the most significant advantages of online courses is their flexibility. With AAPS, you can learn when and where it’s most convenient for you—early in the morning, during a lunch break, or late at night. Our programs include synchronous and asynchronous learning options,.. READ MORE »
Regulatory submissions are a cornerstone of the pharmaceutical industry, and mastering this process is essential for regulatory affairs professionals. On November 8, 2024, AAPS hosted an insightful webinar on Drug Product Submission (NDS) Preparation in eCTD format. The webinar aims to equip participants with practical knowledge and skills for successful submissions. Here are the four key takeaways from this dynamic event. 1. Understanding the Importance of the Common Technical Document (CTD) One of the standout segments of the webinar focused on the Common Technical Document (CTD), a globally standardized format for regulatory submissions. Participants learned how the CTD facilitates organization.. READ MORE »
Canada’s commitment to building a highly skilled workforce includes the Canada-Ontario Job Grant (COJG), a valuable resource for pharmaceutical industry employers looking to invest in developing their teams. Through COJG, companies can access high-quality pharmaceutical training for their employees at our pharmaceutical institute, AAPS. This helps employers keep their teams at the forefront of industry standards. For pharmaceutical companies, COJG offers a cost-effective path to upskill employees, enabling teams to enhance their knowledge and adapt to the industry’s evolving needs. Here’s how this grant supports employer-driven team development. What is the COJG? The Canada-Ontario Job Grant (COJG) program provides financial.. 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 highest quality and safety standards is paramount in the pharmaceutical industry. Good Manufacturing Practices (GMP) regulations provide a critical framework to achieve this goal. However, staying up-to-date on the intricacies of GMP compliance and effectively implementing these principles within your organization can take time and effort. Here at AAPS, we understand these challenges. That’s why we have an annual GMP Masterclass, a comprehensive online workshop designed to equip leaders in the pharmaceutical industry with the knowledge and skills necessary to excel in today’s dynamic regulatory environment. Why Attend the GMP Masterclass? This dynamic online workshop, taking place on.. READ MORE »
The world of pharmaceutical manufacturing demands meticulous attention to detail and unwavering commitment to quality assurance. Atikur Talukder, a leading expert in advanced GMP (Good Manufacturing Practices) and auditing at AAPS embodies these qualities. A seasoned pharmaceutical professional with a rich background in commercial manufacturing, quality assurance, and R&D, Atikur epitomizes the dedication required to achieve and maintain high standards in this field. His journey provides invaluable insights for those aspiring to excel in pharmaceutical manufacturing and quality assurance. In this blog post, Atikur shares his insights on navigating the ever-evolving world of pharmaceutical regulations and offers invaluable advice for.. READ MORE »
The pharmaceutical industry is fast-paced and constantly changing and requires a level of innovation and diligence to be successful. If this sounds like you, then you’ll love the Clinical Research, Drug Safety, and Pharmacovigilance program at AAPS. Our program offers students the opportunity to get hands-on experience with administering and monitoring clinical trials and conducting drug safety and pharmacovigilance activities. Many students go on to fill roles as pharmacovigilance officers at large companies, where they directly apply their studies to their new careers. Gaining experience with encounters you’ll likely have on the job, such as the need to learn Pharmacovigilance.. READ MORE »
