Global Quality Standards – the new approach to compliance documentation

6 years ago Posted By : User Ref No: WURUR23499 0
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  • TypeWebinar
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  • Location Aurora, Colorado, United States
  • Price
  • Date 14-08-2018
Global Quality Standards – the new approach to compliance documentation, Aurora, Colorado, United States
Webinar Title
Global Quality Standards – the new approach to compliance documentation
Event Type
Webinar
Webinar Date
14-08-2018
Last Date for Applying
14-08-2018
Location
Aurora, Colorado, United States
Organization Name / Organize By
Training Doyens
Organizing/Related Departments
Life Science
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Biotechnology

Medical/Healthcare/Hospital

Location
Aurora, Colorado, United States

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.

The approach and philosophy here are new to the industry and focus on achieving maximum benefit of compliance documentation across many applications to achieve both operational efficiencies and compliance excellence. This webinar will address the new thinking as to how documentation hierarchies should be organized to reflect a global focus on how your documentation should be structured.

This webinar will also discuss how to transform your regulatory documentation process a profit center, an operational force multiplier in how you run your business, and an effective central focus of your technical training function

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
  • Explain the best techniques for gathering the technical information you need to develop your documents.
  • Explain how to most effectively work with Subject Matter Experts.
  • Explain how to streamline regulatory document management system and manage technical document reviews

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.
  • Compliance documentation, properly crafted, is a valuable performance management tool for both managers and associates alike.

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: [email protected]

Toll Free: +1-888-300-8494

Tel: +1-720-996-1616

Fax: +1-888-909-1882

 

 

Others Details

Learn how to write standard operating procedures and work instructions and explore the true purpose and function of compliance documents. Also learn about the best techniques for gathering the technical information for documentation.

Registration Fees
Available
Registration Fees Details
Live Session for one participant $199 Corporate Live Session Group – Max 10 Participants from one location. $549 Recorded Session Get unlimited access to the link for six months. $219 Training DVD or USB Flash Drive MP3 files, PDF presentation and reference manual will be delivered on a CD $399 Super Combo Offer 1 Live and Recorded webinar $329 Super Combo Offer 2 Live and Training CD $499
Registration Ways
Email
Phone
Website
Other
Address/Venue
  Training Doyens 26468 E Walker Dr,Aurora, Colorado  Pin/Zip Code : 80016-6104
Landmark
Colorado
Official Email ID
Contact
Training Doyens

26468 E Walker Dr, Aurora, Colorado 80016

[email protected]

   +1-720-996-1616