Are you a quality assurance professional seeking to enhance your expertise in regulatory standards? Don’t miss our upcoming webinar on November 28, 2024! We’ll dive deep into the United States Pharmacopeia (USP), demystifying its complex structure and providing practical guidance for its effective use. Whether you’re a seasoned quality assurance reviewer, a quality control chemist, or a new science graduate, this webinar will equip you with the knowledge you need to navigate the USP confidently and accurately. Why Attend This Webinar? The USP is a critical resource for professionals across the pharmaceutical, cannabis, and herbal drug industries, setting standards to.. READ MORE »
The Canadian Quality Assurance (QA) industry is tough to navigate, requiring more than just technical skills—it takes determination, education, and experience. Aishwarya Venkatasubramanian, a recent graduate of the AAPS Quality Assurance and Regulatory Affairs (QARA) post-graduate diploma program, exemplifies this. In this blog, we explore Aishwarya’s journey from biotechnology to a successful career in Quality Assurance, with comprehensive support from AAPS College. A Passion for Healthcare and Education Aishwarya’s passion for healthcare has driven her journey from completing a master’s in biotechnology in India to navigating new challenges in Canada. Upon arrival, she balanced her personal life and career ambitions,.. READ MORE »
The pharmaceutical and biotech industries are well known for maintaining high standards of quality and compliance, and Quality Assurance (QA) professionals are instrumental in ensuring that products meet the rigorous standards set by regulatory bodies. One of the key resources guiding these professionals is the United States Pharmacopeia (USP), a compendium of drug standards that provides guidelines for product quality, purity, strength, and consistency. Understanding and navigating the USP is essential for QA professionals to ensure compliance and maintain product quality. This blog post explores the USP’s importance and what QA professionals must know to follow its guidelines. The Importance.. 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 »
Quality assurance is a critical aspect of the pharmaceutical industry. Ensuring the safety, effectiveness, and quality of drugs and medical devices is of utmost importance for both consumers and regulatory bodies. Consequently, there is a growing demand for individuals with specialized knowledge and training in quality assurance within the pharmaceutical industry. Whether you’re just starting your career or looking to advance, investing in pharmaceutical training can help you meet the demands of the industry and grow your career. At AAPS, our Pharmaceutical Quality Control and Quality Assurance Post-Graduate Diploma Program has been specifically designed to equip you with all the.. READ MORE »
