The secret to effective compliance documentation and technical training lies in how the analysis is conducted and how training and compliance documentation are developed as a result of that analysis.
Many regulated industries have a multitude of documents to meet their regulatory needs, training materials, SOPs, Work Instructions, Job Aids, and Performance Tests etc. all independently prepared complicating document control and impacting individual document effectiveness.
This webinar will provide the best practice approach for conducting an efficient, effective, and complete documentation and training analysis for a regulated environment as well as developing both training materials and compliance documents that effectively serve a multitude of uses. How well an analysis is conducted impacts cost, the speed of training delivery, and the quality of the regulatory documentation produced.
This webinar will guide the participant through the entire process from start to finish and will discuss how training materials and compliance documentation can be developed to meet complimentary purposes.
Areas to be Covered:
Elements of a regulatory documentation and training program
How regulatory documentation and training are linked
Regulatory compliance documentation hierarchies
Areas of the organization/process that must be examined and analyzed
Conducting the analysis – using subject matter experts
Training task characteristics that impact training delivery
Use of the Analysis Tool to capture the required information
Performance objectives, how they are developed and how they impact the training process
Who will Benefit:
A must attend webinar for all personnel / companies in the Pharmaceuticals, Medical Devices, Biotechnology, Cosmetics, Personal Products, Foods & Beverages fields. The professionals who will benefit include all:
Training Managers and Directors
Product Development Professionals