|
Live Webinar Write effective SOPs & Work Instructions
Everyday 10.00 AM
http://https://worldcomplianceseminars.com/webinardetails/394
Hollywood FL Wisconsin 33021
Report Abuse
|
|
Live Webinar Write effective SOPs & Work Instructions
Description
Standard Operating Procedures – the documentation required by regulation – is 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 those documents 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 unimportant work task.
Areas Covered
• The true purpose and function of regulatory documentation.
• What is the value add?
• The pitfalls associated with writing regulated documentation.
• The documentation hierarchy.
• Documentation formats.
• Gathering the technical information you need.
• Using Subject Matter Experts.
• Documentation writing tips.
• Managing technical document reviews.
Who will Benefit
Quality, production, compliance, engineering, R & D, management – essentially everyone in the organization that is tasked with creating regulatory documentation.
Industries who can attend
This 60-minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.
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.
He has held senior positions in consulting and in corporate training development prior to forming C. H. Paul Consulting, Inc.. He also worked for several years in government contracting managing the development of significant Army-wide training development contracts impacting virtually all of the active Army and changing the training paradigm throughout the military.
He has dedicated his entire professional career explaining the benefits of performance-based training
$179 One Dial-in One Attendee|$279 One Dial In - Max 10 attendees |$695 Multiple locations upto 5 dial in|$249 Available within 24 hrs after |$299 CD/DVD will be dispatched after |
https://worldcomplianceseminars.com/webinardetails/394 |
conference manager Phone: 08442677299 Email: subscribe (at) worldcomplianceseminars.com |
|
|
| Report Abuse |
|
|
| |
| |
|
| List your Event |
| | Similar Events | Barcelona: 11th International Conference on Epilepsy & Treatment Welcome to The 11th International Conference on Epilepsy & Treatment which is going to be held during April 29-30,2025 is a significant event in the field of neurology and epilepsy care, set to take place in the culturally rich and vibrant city o Date Posted: 04-Nov-24
| Barcelona: 11th International Conference on Epilepsy & Treatment About Conference
Welcome to The 11th International Conference on Epilepsy & Treatment which is going to be held during April 29-30,2025 is a significant event in the field of neurology and epilepsy care, set to take place in the culturally r Date Posted: 23-Nov-24
| FL: Live Webinar Write effective SOPs & Work Instructions Live Webinar Write effective SOPs & Work Instructions
Description
Standard Operating Procedures – the documentation required by regulation – is essential to the effective and compliant running of any regul Date Posted: 02-May-18
| Boston: 2 DAY SEMINAR Effective Compliance Strategies for Complaint Handling, 2 DAY SEMINAR Effective Compliance Strategies for Complaint Handling, Medical Device
Location 1: Boston,MA
Jul 11 - 12
Description
Complaint handling systems have come under intense scrutiny by the FDA in recent years and enforcement trends Date Posted: 04-May-18
| FL: Conducting a life sciences documentation and training gap analysis Conducting a life sciences documentation and training gap analysis
Description
The relationship between government regulations, actual job tasks performed by workers, compliance requirements, equipment maintenance and operational requirements, Date Posted: 29-May-18
| FL: Conducting a life sciences documentation and training gap analysis Conducting a life sciences documentation and training gap analysis
Description
The relationship between government regulations, actual job tasks performed by workers, compliance requirements, equipment maintenance and Date Posted: 27-Apr-18
| FL: Live Webinar Understanding and Applying the New EU Medical Device Regu Live Webinar Understanding and Applying the New EU Medical Device Regulations (EMDR)
Description
The European Parliament just adopted the Medical Devices (MDR) and In vitro Diagnostic Medical Devices (IVDR) regulations. The adoption Date Posted: 26-Apr-18
| FL: Live Webinar The prevention of human error in pharmaceutical manufactu Live Webinar The prevention of human error in pharmaceutical manufacturing
Description
This webinar will explore the true causes and nature of human error, how human error should be investigated, how human error relates to Date Posted: 02-May-18
| FL: Live Webinar The prevention of human error in pharmaceutical manufactu Live Webinar The prevention of human error in pharmaceutical manufacturing
Description
This webinar will explore the true causes and nature of human error, how human error should be investigated, how human error relates to Date Posted: 02-May-18
| FL: 3-hrs Webinar-Deciding When to Submit a 510(k) for a Change to an Exis 3-hrs Webinar-Deciding When to Submit a 510(k) for a Change to an Existing Device – FDA’s Final Guidance
Description
A premarket notification (510(k)) is required when a legally marketed device subject to 510(k) requirements is about to be Date Posted: 30-Apr-18
| FL: 3-hrs Webinar-Deciding When to Submit a 510(k) 3-hrs Webinar-Deciding When to Submit a 510(k) for a Change to an Existing Device – FDA’s Final Guidance
Description
A premarket notification (510(k)) is required when a legally marketed device subject to 510(k) requirements is about to b Date Posted: 11-May-18
| FL: Live Webinar Construct and Manage the Technical File and Design Dossie Live Webinar Construct and Manage the Technical File and Design Dossier
Description
This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the glo Date Posted: 30-Apr-18
| FL: 3-hrs Virtual Training 2018 Latest FDA thinking on deciding when 3-hrs Virtual Training 2018 Latest FDA thinking on deciding when to Submit a 510(k) for a Change to an Existing Device – FDA’s Final Guidance
Description
A premarket notification (510(k)) is required when a legally marketed device subject Date Posted: 31-May-18
| FL: Live Webinar FDA’s Final Rule Regarding Device Establishment Registrat Live Webinar FDA’s Final Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List
Description
Device firms, establishments or facilities that are involved in the production and distribution of medica Date Posted: 08-May-18
| FL: Live Webinar FDA Compliance and Mobile Applications Description
Computer system validation has been regulated by FDA for more than 30 years, as it relates to systems used in the manufacture, testing, distribution and management of a product in the pharmaceutical, biotechnology, medical device, tobacc Date Posted: 26-Apr-18
|
|
Map locations are shown as per geocoding services and they depeneds on the accuracy of the address. If address is wrong it may show wrong map. If you put a listing which shows wrong map, please remove the listing and create a new one with correct address details.
Please note: The information on this site is submitted by users. CanadianDesi never checks accuracy of the information. Please use this information at your risk. If you have any question or concern regarding this listing, or you know that the above information is not accurate, please Contact Us. Thanks.
|
| Please note: The information on this site is submitted by users. CanadianDesi never checks accuracy of the information. Please use this information at your risk. If you have any question or concern regarding this listing, or you know that the above information is not accurate, please Contact Us. Thanks.
|
|