Showing posts with label basics. Show all posts
Showing posts with label basics. Show all posts

Sunday, July 24, 2016

GMP Basics for Beginners & Experienced Team Members - cGMP Training Course

cGMP Basics Training Course for Beginners, and Experienced Professionals


Naturally you'll want your new hires introduced to the basics of the FDA cGMP regulations.

Don't forget that your experienced team members need occasional doses of GMP refresher training too!

You might be interested in our cGMP training course:

Thursday, February 5, 2015

CGMP Training - GMP Essentials for Drug Manufacturers

Updated Febrruary 27, 2026:

The original link broke.


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GMP Essentials for Drug Manufacturers - An Onsite GMP Training Course

Intended for: 

  • new employees and non-cGMP transfers who need basic cGMP training, or
  • current staff or those individuals needing refresher training.

This highly interactive course gets everybody talking about current CGMP practices, underlying laws and regulations, the consequences of non-compliance, and recent trends. Many CGMP principles are experienced hands-on in this session. This course is usually customized to meet the needs of the organization, and can be designed to run over 1-3 days. Call (415) 948-5220, to discuss your specific needs. 

Read the feedback:

  • The exercises were great! 
  • The lack of excessive breaks was a great time saver.
  • Lively and friendly
  • The instructor's experience was very helpful. 
  • Group activities helped in the learning. 
  • It never dragged on. 
  • Allan seems to know when to move on. 
  • Teacher was great! 
  • Content explained clearly 
  • A nice balance of PowerPoint and activities 
  • This class helped me see where we need to make changes in what we are doing. 

Learn more about this onsite cGMP training course, GMP Essentials for Drug Manufacturers - GMP training by SkillsPlus Intl Inc. 

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SkillsPlus Intl Inc. - The Best GMP & QSR Compliance Training Around

Thursday, November 14, 2013

GMP Training - The cGMP Essentials Course

Updated October 31, 2024

The original post didn't age very well.

You might also be interested in:


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483 Observation Gotchas!
 
1. There is no documented training in CGMPs.
2. CGMP training has not been conducted for over three years.
3. Firm lacks qualified CGMP trainers. 
 
 
Planning for Training 2014!

 2014 is just around the corner! 
  1. Do you need to get CGMP and related training completed and do not have the staff, or
  2. Are you and your staff already overloaded, or
  3. Do you just need a new and exciting approach to CGMP training?

    If you answered "Yes" to one or more of these questions, then take a look at our CGMP Essentials course.
Learn More About the SkillsPlus CGMP Essentials course
 

Featured Course
CGMP Essentials: This course can be structured with more than two dozen different training activities designed to reinforce learning and keep employees engaged. Prior students have high praise. One manager said, "I never knew CGMP training could be so much fun." One former FDA Inspector reported, "I actually learned something."
 
Topics addressed in this very popular course:
1. Heard on the Street
2. Review of 21 CFR 211 Subparts
3. Essential Quality System Tools
4. Consequences for non-compliance, and more!
 
If your firm needs a fresh new look at CGMP training, then you need to look into our CGMP Essentials course!
 
Examine The CGMP Essentials Course Outline



Monday, February 27, 2012

Essentials for Medical Device Manufacturers - QSR training class

Updated June 5, 2025

This specific course is no longer offered.

You might also be interested in these online training programs:

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In this original or refresher training, experience fun learning the regulations.

Essentials for Medical Device Manufacturers by SkillsPlus International Inc. is an instructor-led training class, taught on-site in-house at client plant locations.  This is useful as a new employee basics course, and can be used as a refresher course.

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

Objectives:
Upon class completion, 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.

Topics:
  • Heard on the street
  • Past, present, and future
  • Legal issues
  • Personnel responsibilities
  • Standard operating procedures
  • Contamination
  • Personal hygiene
  • Cleaning
  • Documentation
  • Materials
  • Process control
  • Buildings and facilities
  • Equipment
  • Validation
  • Calibration
  • Laboratory
  • Quality management system
For more information about this class:
Essentials for Medical Device Manufacturers by SkillsPlus International Inc

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

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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