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Global Quality Standards – the new approach to compliance documentation

Event Details

Global Quality Standards – the new approach to compliance documentation

Time: August 14, 2018 from 1pm to 2pm
Location: Training Doyens 26468 E Walker Dr
Street: 26468 E Walker Dr, Aurora, Colorado 80016
City/Town: Aurora
Website or Map: https://bit.ly/2J7QrcY
Phone: +1 720-996-1616
Event Type: webinar
Organized By: Training Doyens
Latest Activity: Jul 10

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Event Description

OVERVIEW

Standard Operating Procedures and work instructions – the compliance documentation required by regulation – are essential to the effective and compliant running of any regulated business. Unfortunately, many individuals in those businesses miss the valuable opportunities that properly developed Standard Operating Procedures/Work Instructions can provide.  Regulated documentation can serve a variety of purposes other than meeting a regulatory requirement – as training materials, to standardize operations, to manage individual and group performance, to identify the sources of deviations, etc.  The key is to knowing how to write standard operating procedures and work instructions to properly meet those needs.

WHY SHOULD YOU ATTEND

Writing effective Standard Operating Procedures and Work Instructions is not intuitive, it is not a skill that is often taught in our universities, and it can be a difficult and cumbersome task to execute. Knowing the most effective and efficient processes for gathering, organizing, and writing technical documentation is absolutely critical to providing significant value to a dreaded, avoided, and seemingly (and wrongfully) unimportant work task.

AREAS COVERED

  • Define the true purpose and function of regulatory documentation.
  • Determine the value add that regulatory documentation can bring to your organization.
  • Identify the pitfalls associated with writing regulated documentation.
  • Explain the purpose and function of a documentation hierarchy – and the new global thinking concerning documentation hierarchies.
  • Explain how documentation is created.
  • Identify and explain the best types of formats that can used to develop standard operating procedures and work instructions

LEARNING OBJECTIVES

  • Compliance documentation should never be developed to simply meet a regulatory requirement.
  • Compliance documents, properly crafted, can significantly minimize the training burden faced by life sciences companies today.
  • Compliance documents, properly crafted, can virtually eliminate the potential for deviations throughout the operation.

WHO WILL BENEFIT

Anyone tasked with the development of regulatory documentation in any regulated industry -  the Life Sciences (medical devices, pharmaceuticals, biologics, etc), foods, cosmetics, beverages, nutraceuticals, etc.

This webinar has a very broad base from which to solicit participants.  Virtually any regulated industry as previously defined and virtually any job classification level – associates through managers and in virtually any organizational function – operations, facilities, logistics, purchasing, laboratory, research and development, engineering, maintenance, etc.

 

For more detail please click on this below link:

https://bit.ly/2L7BgCb

 Email: support@trainingdoyens.com

Toll Free: +1-888-300-8494

Tel: +1-720-996-1616

Fax: +1-888-909-1882

 

 

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