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Validity : 18th Sep'25 to 28th Sep'25
This training on FDA software validation and verification will provide you with the best practices necessary to ensure that all systems are validated in compliance with FDA regulations.
This webinar will define what are the US FDA's expectations for proper laboratory / clinical / manufacturing practices, systems, equipment usage, and documentation / record-keeping. It will evaluate the requirements for how basic Quality Management System (QM ...
Mapping and evaluating all the steps in a pharmaceutical warehousing and distribution workflow can lead to valuable process improvements. In this webinar, we discuss how this review can be accomplished and the possible benefits that can result.
What is discrete event simulation modelling for resource utilization and staffing & scheduling problems Why and when to use simulation modelling for resource utilization and staffing & scheduling problems Input information required by a typical simulatio ...
As of August 1, 2023, the Form I-9 has been updated to include a remote verification option. This webinar will review the changes in detail and how the employer can deal with them. We also have additional options of going electronic with the Form I-9. This we ...
Policymakers and payers have grown increasingly frustrated with fee-for-service payment system. Fee-for-service rewards volumes and encourages silos and fragmentation of care. There are a lot of efforts that seek to shift provider payments to value-based appro ...
This webinar is focused on the workings of the Quality Management System, what is required of a compliant system according to ISO 9001, and the QMS audit. This seminar will evaluate the requirements for the foundational / basic Quality Management System (QMS), ...
Supervision plays a crucial role in Human Error Reduction and Control. Critical Factors like preparation, planning, scheduling, communication, among many others, will be discussed as part of this webinar. People make mistakes because they can; our systems allo ...
In Good Manufacturing Practice (GMP) environments, human error is a persistent challenge that can lead to deviations, batch failures, regulatory non-compliance, and even product recalls. Studies show that over 70% of GMP deviations are attributed to human erro ...
This webinar will discuss the best practices for the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.