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Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations

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Website https://tinyurl.com/ydz8tzqn | Edit Freely

Category bank compliance risk assessment matrix, bank compliance risk assessment template

Deadline: November 30, 2017 | Date: November 30, 2017

Venue/Country: CO, U.S.A

Updated: 2017-11-06 18:54:08 (GMT+9)

Call For Papers - CFP

OVERVIEW

When there is a need to make some change to an environment and/or resolve a problem, we must think about a project that could implement the necessary change and address the problem. But we can’t just run our project without proper justification. Justifying the project is a great mechanism to confirm that our project really addresses the need and paves the way for improvement. It helps us assure interested parties or stakeholders that the project implements a particular solution to the problem and explains why this solution is best, as compared to other alternative solutions.

But how do we do a project justification? In this webinar, you will learn about analyses which are regarded as compliant and convenient ways to justify and confirm projects such as Change Controls, Risk Assessments, Validations, and Investigations.

WHY SHOULD YOU ATTEND

As regulations change and become more stringent, one aspect of compliance has not changed, and that is ensuring changes, deviations, validations and risk assessments are done properly and have a proper justification and rationale. It is easy to document what process has been performed, what has been investigated or changed or why something is a risk, but the difficult part knows how to explain or justify why it should be done or why a product should be released or rejected as a result. In this webinar, you will learn efficient and complaint ways to justify the validations, changes or deviations in a manner that will explicitly demonstrate to the reader why the process was performed the way it was.

AREAS COVERED

• How to propose a solution to the problem related to the deviation, change control, risk assessment or validation study

• Determine alternatives or options to the proposed solution

• Analyze costs, benefits, impacts, and risks of the proposed solution

• Validate the solution, assess product impact to the market

• Determine impact to the patient, system or firm as a result of your findings

WHO WILL BENEFIT

• Quality Assurance/

• Quality Control Directors,

• Managers, and Specialists

• Regulatory Affairs/Regulatory

• Compliance Directors, Managers, and Specialists

• Engineering/Development Directors, Managers, and Specialists

LEARNING OBJECTIVES

• After attending this webinar, participants will:

• Be able to plan an investigation, change control, risk assessment or validation relevant to the area of study

• Be able to undertake the planned investigation, change control, risk assessment or validation using appropriate scientific principles

• Be able to collect, collate and analyze the results from the investigation, change control, risk assessment or validation

• Be able to draw conclusions from the investigation, change control, risk assessment or validation

For more detail please click on this below link:

https://goo.gl/RqJ7J6

Email: support@trainingdoyens.com

Toll Free: +1-888-300-8494

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Fax: +1-888-909-1882


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.