Showing posts with label location. Show all posts
Showing posts with label location. Show all posts

Friday, April 12, 2013

Root Cause Analysis for Better Deviation Investigations - Onsite Courses - Popular

These highly popular cGMP & QSR training classes are taught at the location of your choice, as a client on-site in-house training. You might be interested in two of our highly inter-related courses.
  1. Root Cause Analysis for Better Investigations, and
  2. Deviation Investigation Reports
- - - FIRST - - -

Root Cause Analysis for Better Deviation Investigations: On-site Training by SkillsPlus International Inc.:
"Purpose:
  • To conduct or facilitate an individual or team-based investigation that solves problems and gets results, and complies with FDA expectations in the pharmaceutical and biotech industries. 
Objectives
1. Use tools and techniques to effectively identify the deviation statement.
2. Identify the root cause of the deviation.
3. Generate and objectively select the best corrective and preventive actions.
4. Assess the risk of implementing the corrective action and preventive action.
5. Develop a contingency plan to preventive action implementation.
6. Create corrective actions and preventive action metrics. 
About the Class
1. This class uses current deviations to practice the techniques taught.
2. The optional final exam is approximately 25 questions.
3. Each student receives a student guide containing a representation of the program's
slides and graphics with space provided for note taking.
4. This class can accommodate up to 25 people.
5. Duration: 8 hours."
'via Blog this'

- - - SECOND - - -

Deviation Investigation Reports: On-Site Training by SkillsPlus International Inc.:

Purpose:
  • To use the data collected in an investigation to write a report and answer management and FDA questions.
 Objectives 
  1. Increase investigation report suitability for FDA review. 
  2. Decrease the number of reports returned by internal reviewers. 
  3. Write supported deviation statements. 
  4. Provide a detailed background statement to include related information, investigations, affected materials and references. 
  5. Document deviation investigation findings. 
  6. State the root cause with supporting facts. 
  7. Generate supported, plausible, and defensible corrective actions. 
  8. Develop effectiveness measures for the corrective actions. 
  9. Generate realistic preventive actions. 
  10. Develop effectiveness measures for the preventive actions. 
  11. Develop a follow up plan for corrective and preventive actions. 
  12. Write accurate executive summary statements. 
 About the Class
  1. In-house deviation reports will be used to demonstrate and practice the skills and principles of this class.
  2. This course is best taught in a computer lab. We can ship computer labs to your site if needed.
  3. This course is customized to reflect your company procedure on writing deviation investigation reports. As we review that document we will make any recommendations to for change that we feel would be helpful.
  4. The optional final exam is approximately 25 questions.
  5. Each student receives a student guide containing a representation of the program's  slides and graphics with space provided for note taking.
  6. This class can accommodate up to 12 people.
  7. Duration: 8 hours as a minimum.
For more information:

Return to SkillsPlus International Info Blog - Home

SkillsPlus Intl Inc. - GMP & QSR Compliance Training Experts website

Thursday, April 12, 2012

Qualstar Simulation - Advanced QSR & GMP Training Onsite

Qualstar Simulation: CGMP or QSR Advanced Onsite Training Course by SkillsPlus Intl Inc

This highly interactive on-site training class is action packed and keeps students energized. Students actually have fun while learning!

This is an instructor led course taught onsite, in-house, at client locations.  Students learn about the importance of documentation, procedures, change control and QA.

By the end of class, participants will be able to:
  1. demonstrate proper documentation practices. 
  2. experience the value of well-written procedures. 
  3. demonstrate proper actions when procedures contain errors. 
  4. experience the value of the quality unit.
Get your employees excited about learning and training with this exciting and engaging class!

Learn more about this live training class:

Return to SkillsPlus International Info Blog - Home

SkillsPlus Intl Inc. - GMP & QSR Compliance Training Experts website

Thursday, March 1, 2012

Essentials for Pharmaceutical Manufacturers - Live onsite cGMP training

Updated July 16, 2021

Links in the original post broke.

You might also be interested in:

---   the original post follows below   ---

Essentials for Pharmaceutical Manufacturers is a SkillsPlus International Inc. course - it's a live onsite cGMP training class taught on-site, in-house, at client plant locations.

It's the perfect introductory class for employees new to the pharma-biotech industry, and also serves as a wonderful refresher course for staff needing continuing education.

By the end of this engaging interactive class, students will be able to:
1. State the historical development of CGMP regulations.
2. Explain the role and function of standard operating procedures.
3. Describe the personal role for contamination control.
4. Identify the sources of contamination.
. . . and much more!

For more information, go to:
Essentials for Pharmaceutical Manufacturers is a SkillsPlus International Inc. course

Return to SkillsPlus International Info Blog - Home

Tuesday, February 7, 2012

Faster Product Release Through Efficient Batch Record Review - Onsite cGMP & QSR Training Class

Updated March 17, 2023

The batch record review course is no longer available.


---  the original post follows below  ---

Faster Product Release Through Efficient Batch Record Review - Live onsite cGMP & QSR training by SkillsPlus International Inc.

This is a live on-site class. It is instructor-led and taught at the client location of your choice.

Purpose:
This live on-site GMP & QSR training class teaches students how to competently review batch records to identify errors and issues.

Objectives:
Upon course completion, students will be able to:
 1. State the source of batch record requirements for both US and EU
 2. Distinguish between the production and QA batch record review
 3. List best practices in Batch Record Review
 4. Demonstrate at least 5 different batch record review activities.

Topics include:
  1. Regulation review 
  2. US & EU Requirements and Regulatory Expectations 
  3. Best Practices 
  4. BPR Regulations Background 
  5. BPR Audit Items: Skills Practice 
  6. Trending
For more information, visit:
Faster Product Release Through Efficient Batch Record Review - Live onsite cGMP & QSR training by SkillsPlus International Inc.

Return to SkillsPlus International Info Blog - Home

SkillsPlus Intl Inc. - GMP & QSR Compliance Training Experts website
Additional Keywords: biotech, cGMP, class, compliance, device, DME, drug, energizing, engaging, exciting, FDA, GMP, instructor, interactive, manufacturer, medical, ,pharmaceutical, QSR, SkillsPlus, trainer, training,


Wednesday, January 25, 2012

Root Cause Analysis for Better Deviation Investigations - Live onsite GMP & QSR training

Don't miss this popular course. This cGMP & QSR training class can be taught at the location of your choice, as a client on-site in-house training.

Root Cause Analysis for Better Deviation Investigations: On-site Training by SkillsPlus International Inc.:
"Purpose:
To conduct or facilitate an individual or team-based investigation that solves problems and gets results, and complies with FDA expectations in the pharmaceutical and biotech industries. 
Objectives
1. Use tools and techniques to effectively identify the deviation statement.
2. Identify the root cause of the deviation.
3. Generate and objectively select the best corrective and preventive actions.
4. Assess the risk of implementing the corrective action and preventive action.
5. Develop a contingency plan to preventive action implementation.
6. Create corrective actions and preventive action metrics. 
About the Class
1. This class uses current deviations to practice the techniques taught.
2. The optional final exam is approximately 25 questions.
3. Each student receives a student guide containing a representation of the program's
slides and graphics with space provided for note taking.
4. This class can accommodate up to 25 people.
5. Duration: 8 hours."
'via Blog this'

For more information:
Root Cause Analysis for Better Deviation Investigations: On-site Training by SkillsPlus International Inc.

Return to SkillsPlus International Info Blog - Home

SkillsPlus Intl Inc. - GMP & QSR Compliance Training Experts website
Additional Keywords: affordable, cGMP, class, compliance, device, drug,energizing, engaging, exciting, FDA, GMP, interactive, manufacturer, medical, pharmaceutical, QSR, SkillsPlus, training


Tuesday, January 24, 2012

Live Onsite QSR Training - Olympics for Medical Device Manufacturers

Updated January 10, 2025

The "Olympics" course is no longer available.

You might also be interested in:
https://gmpprof.com/cgmp-training-a-new-generation/

---  the original post follows below  ---

Olympics for Medical Device Manufacturers - onsite QSR training by SkillsPlus International Inc. is an exciting, energizing, and engaging on-site class that can be held at a client in-house location.

This challenging class takes QSRs to a deeper level of understanding through a series of challenging activities.

Upon class completion, students will be able to:
  1. List the hottest issues in QSR compliance. 
  2. Locate items of interest in 21CFR820. 
  3. Explain the 21CFR211 rationale for specific 483 observations. 
  4. Demonstrate knowledge of common CGMP practices and details. 
  5. State the consequences of not following QSR.
For more information:
Olympics for Medical Device Manufacturers - onsite QSR training by SkillsPlus International Inc.

Return to SkillsPlus International Info Blog - Home

SkillsPlus Intl Inc. - GMP & QSR Compliance Training Experts website
Additional Keywords: affordable, class, compliance, course, device, energizing, engaging, exciting, FDA, interactive, manufacturer, medical, QSR, SkillsPlus,

Monday, January 23, 2012

Live Onsite GMP Training - Olympics for Pharma & Biotech Manufacturers

Updated December 7, 2021

The live training course referenced in the original post has been discontinued.


---  the original post follows below  ---

Exciting, energizing, engaging, live client site class held at your location.
Olympics for Pharmaceutical and Biotech Manufacturers - On-site cGMP Training by SkillsPlus International Inc.

This class takes CGMPs to a deeper level of understanding through a series of challenging activities.

Upon class completion, students will be able to:
  1. List the hottest issues in CGMP compliance.
  2. Locate items of interest in 21CFR211. 
  3. Explain the 21CFR211 rationale for specific 483 observations. 
  4. Demonstrate knowledge of common CGMP practices and details. 
  5. State the consequences of not following CGMPs.
For more information:
Additional Keywords: affordable, biotech, cGMP, class, compliance, computer, computer-based training, cosmetics, course,drug,energizing, engaging,exciting, FDA, GMP, instructor, interactive, manufacturer,pharmaceutical,SkillsPlus, training

Wednesday, January 18, 2012

Live Onsite QSR Training - Essentials for Medical Device Manufacturers

Here's one of our popular onsite QSR training classes:
Essentials for Medical Device Manufacturers by SkillsPlus International Inc.

This live class can be taught at the client site location of your choice.

This class teaches employees how to identify the essential elements of QSR for beginning work in the medical device industry.

Upon completion of this class, students will be able to:
  1. State the historical development of QSR regulations. 
  2. Explain the role and function of standard operating procedures. 
  3. Describe the personal role for contamination control. 
  4. Identify the sources of contamination. 
  5. List the common QSR documentation practices. 
  6. Explain material controls. 
  7. State the common practices of production and process controls. 
  8. Explain the importance of an adequate, appropriate, and sufficient building design. 
  9. State the requirements of equipment design and construction. 
  10. List the requirements for building, and equipment cleaning and maintenance. 
  11. Explain the role of the quality management system. 
  12. Explain the role of the laboratory.
Learn more about this class:
Essentials for Medical Device Manufacturers - On-site training by SkillsPlus International Inc.

Return to SkillsPlus International Info Blog - Home

SkillsPlus Intl Inc. - GMP & QSR Compliance Training Experts website
Additional Keywords: affordable, biotech, cGMP, class, compliance, computer, computer-based training, cosmetics, course,drug,energizing, engaging,exciting, FDA, GMP, instructor, interactive, manufacturer,pharmaceutical,SkillsPlus, training

Monday, January 16, 2012

Live Onsite GMP Training - Essentials for Pharmaceutical Manufacturers

Updated November 8, 2022

The links in the original post broke.

You might also be interested in:

---  the original post follows below  ---

Here's one of our popular onsite cGMP training classes:
   Essentials for Pharmaceutical Manufacturers - cGMP training by SkillsPlus Intl Inc.

This live class can be taught at the client site location of your choice.

This class teaches employees how to identify the essential elements of CGMP for beginning work in the pharmaceutical and biotech industries.

Upon completion of this class, students will be able to:
  1. State the historical development of CGMP regulations. 
  2. Explain the role and function of standard operating procedures. 
  3. Describe the personal role for contamination control. 
  4. Identify the sources of contamination. 
  5. List the common CGMP documentation practices. 
  6. Explain material controls. 
  7. State the common practices of production and process controls. 
  8. Explain the importance of an adequate, appropriate, and sufficient building design. 
  9. State the requirements of equipment design and construction. 
  10. List the requirements for building, and equipment cleaning and maintenance. 
  11. Explain the role of quality assurance. 
  12. Explain the role of quality control.
Learn more about this class:
Essentials for Pharmaceutical Manufacturers - cGMP training by SkillsPlus Intl Inc.

Return to SkillsPlus International Info Blog - Home

SkillsPlus Intl Inc. - GMP & QSR Compliance Training Experts website
Additional Keywords: affordable, biotech, cGMP, class, compliance, computer, computer-based training, cosmetics, course,drug,energizing, engaging,exciting, FDA, GMP, instructor, interactive, manufacturer,pharmaceutical,SkillsPlus, training