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.
Technical Writing generally conforms to Good Documentation Practices (GDocP). This term describes standards to create and maintain documents. Also addressed in the webinar are principles to create Technical Documents. Most companies have in-house requirements ...
Problem Solving is a practical business tool used by leading firms. It utilizes the experience of the personnel involved in the situation negatively impacting the desired result. The tools used in the process are probing and effective in getting results. Ha ...
Ethical purchasing includes keeping a level playing field and avoiding giving a vendor the impression that you as a procurement professional may not be impartial. What hidden signs to look for and what company policies may need to be instituted to keep or limi ...
Uses and abuses Resilience of materials Resilience applied to financial institutions The stages in handling shocks Stress-testing: an ex-ante view Resilience and bank supervision Resistance vs. resilience Crisis management Towards the optimal way to ...
PivotTables can help you sort and sift through large data sets to focus quickly on just the data elements that matter most to your specific needs. In just one fast-paced and informative training session, you’ll learn how to use PivotTables to sort your data m ...
Running an effective job interview is essential to getting the right candidate. To be a good interviewer, you also have to be prepared, ask the right questions, listen, and evaluate the candidate. Hiring someone "like you" isn't necessarily going to get you th ...
The objective of the webinar is to present suggestions and hints to create Policies, Processes, and Procedures that can be applied to various fields and/or departments of organizations. Many fields can benefit from learning how to create Policies, Processes, ...
FDA requires that all computer systems used to produce, manage and report on “GxP” (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. This webinar will help you understand the FDA’s current thinking on computer sys ...
This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud-hosted applications. It explains how to write a Data Privacy Statement for compliance with EU General Data Protection Regulat ...