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 ...
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human performance problems can be prevented. Human errors start at the design stage. Proced ...
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 ...
Assessment of the cause for non-compliance is a structured series of branching questions. The answers to these eliminate possibilities and eventually highlight a root cause. This process is described, including roles and responsibilities, timing, and efforts a ...
This webinar will focus on the cybersecurity of medical devices, a key concern for those who develop, manufacture, test, and distribute these products. Protecting medical devices from hacking where someone can alter the actual code embedded in the device coul ...
This webinar is about scheduling and how to structure a project schedule that works and ensures the accomplishment of the project’s objectives. Participants will be walked through the scheduling process from start to finish in language that will clearly descr ...
Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction, and monitoring of a compressed air system are essential for maintaining a quali ...
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, ...
This webinar will examine the existing and proposed requirements for the U.S. FDA's DHF -- including its derivitive documents, the DMR and DHR.It will consider the European Union's MDD TF/DD requirements currently being phased out and the new EU MDR Technical ...
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 ...