ISPE serves as the catalyst for solutions that influence global public health and ensure the safety of the world's supply of medicines through its many training resources. In order for ISPE to maintain its position as the go-to resource by manufacturing professionals and regulators worldwide, you are invited to participate in this brief 17-question survey about your training needs. Simply click on the link below, or cut and paste the entire URL into your browser to access the survey. We would appreciate your response by 30 June 2015. Your input is very important to us, and will help us develop training courses that will help you maintain product quality and meet regulatory requirements. Thank you in advance for your time and participation.
In the pharmaceutical industry, which is highly regulated, aseptic processing is a critical component that ensures the sterility of products. Regulators have a set of comprehensive requirements that minimize the risk of contamination. Regulators set the requirements; however, the industry has an obligation to the patients who rely on and expect a drug that is safe and free of contamination....
Like any investment in digital manufacturing systems, demonstrating business payback before and after investment is critical to getting MES projects approved and verifying profitability after investment. Whether it is introducing MES, expanding it to additional sites, switching software, upgrading existing software, or developing electronic production records (EPR) for new drug products,...
Sustainability is emerging as a pivotal force influencing the pharmaceutical industry’s dynamics and steering companies towards transformative change. The focus of this analysis is to delve into the sustainability key performance indicators (KPIs) of prominent pharmaceutical players, namely Pfizer, Sanofi, Glaxo Smith Kline (GSK), Becton Dickinson, Johnson & Johnson, Abbott, Eli Lilly, and...