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Conducting a life sciences documentation and training gap analysis

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Website https://worldcomplianceseminars.com/webinardetails/391 | Edit Freely

Category

Deadline: May 18, 2018 | Date: May 18, 2018

Venue/Country: Online, U.S.A

Updated: 2018-05-08 16:22:24 (GMT+9)

Call For Papers - CFP

Conducting a life sciences documentation and training gap analysis

Time: 03:00 PM EDT | 12:00 PM PDT | 02:00 PM CDT Duration 60 Minute

Description

The relationship between government regulations, actual job tasks performed by workers, compliance requirements, equipment maintenance and operational requirements, and process descriptions all are foundational to both the training that must be conducted in a regulated facility and the actual compliance documents that must be created to meet all regulatory requirements. How a training and documentation professional undertakes an analysis to determine these requirements directly influences the quality of the training developed and fielded and the completeness and relevance of the compliance documentation prepared.

Why should you attend :

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.

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 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

Anyone involved in the design and development of medical devices and pharmaceuticals from R & D, compliance, training, regulatory, and engineering.

Speaker Profile

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, manufacturing, training, and technical documentation consulting firm – celebrating its twentieth year in business in 2017. Charles has been a regulatory and management consultant and an Instructional Technologist for 30 years and has published numerous white papers on various regulatory and training subjects. The firm works with both domestic and international clients designing solutions for complex training and documentation issues.

Price: $179 One Dial-in One Attendee | Corporate Live Recorded $279 One Dial In - Max 10 attendees |Group $695 Multiple locations upto 5 dial in | Recorded $249


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.