BSI Consulting training

Understanding the C-TPAT program requirements, benefits, how to maintain compliance, and prepare for validations can be overwhelming. On the surface the C-TPAT program and application seem to be straightforward however, at times it can become quite complicated. Not knowing where to start or how to begin the initial application process is something some companies tend to struggle with along with developing and documenting a risk assessment program to meet C-TPAT`s standards. To become certified and maintain it, it`s important that you have a reliable resource to guide you through the process and help you identify current security gaps within your program, so they don&apos:t affect your status in the program.

For Pharmaceutical manufacturers to overcome challenges, such as consumer health concerns, damaged brand and reputation, financial loss and regulatory action, it`s vital that organizations have a robust quality and risk management program in place to monitor and track supplier compliance with GMP and other regulatory requirements. Solid quality management programs can greatly reduce the occurrence of quality issues and other impacts, and maintain product quality. The first step to developing a reliable program is to understand GMP regulations and where the gaps exist within your program in order to take action to mitigate those exposures. This training will help your organization understand GMP regulatory requirements, and how to design implement a solid management program to ensure supplier compliance.