GMP eLearning  Online Courses

About Our Online Training Courses

  • $50 per individual course. Once a course is purchased, you’ll be able to view the course one-time (within 48 hours from the time of purchase).
  • Call us about Annual Global License pricing:  (415) 948-5220

Courses Currently Available

  • 21 CFR 211: Pure, Safe, and Effective – This program reviews 21 CFR 211 with the reminder that all these rules help us produce a product that is pure, safe and effective. This program is a must for new employee orientation training at all levels of the organization.
  • Documentation Practices – This program provides a most interesting review of proper documentation practices for both paper-based and electronic record environments.
  • Equipment and CGMPs – This topic discusses the requirements of 21 CFR211 Subpart D – Equipment, specifically the design and construction requirements for equipment including lubrication and coolants. The class addresses cleaning and maintenance requirements including automatic and electronic equipment. The class also covers the requirements for equipment identification, and required documentation.

Courses Coming Soon

  • Buildings and Facilities
  • Surviving an FDA Inspection
  • Understanding Validation
  • Contamination Control
  • Materials and CGMP
  • Organization and Personnel
  • Production and Process Control
Online FDA cGMP QSR GMP Training Courses
Online FDA cGMP QSR GMP Training Courses – Give us a call:  (415) 948-5220

You might also be interested in:
GMP Training – Courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

Medical Device Tax Is History After Trump Signs Repeal – BioFlorida

According to the article:

“The medical device industry hailed President Trump’s signing into law a bipartisan federal spending package that brings in an end to a tax the medical technology industry has been fighting against for the last decade.

The 2.3% tax on medical device sales that is part of the Affordable Care Act has already been on temporary hiatus since the beginning of 2016, but was scheduled to return at the end of this year if Congress didn’t eliminate the tax or put it on hiatus once again.”

Read the full source article:  Medical Device Tax Is History After Trump Signs Repeal – BioFlorida

You might also be interested in:
GMP Training – Courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

FDA cGMP QSR GMP Online Training Courses by SkillsPlus Intl Inc.

cGMP, QSR, GMP online training courses taught by SkillsPlus International Inc.

Learn more about our most popular online training courses:

  • Root Cause Analysis and Investigation Report Writing – Online Self-Study
  • GMP Trainer Awareness, Certification, and Master Trainer Course
  • Online e-Learning Courses

You might also be interested in:
GMP Training – Courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

Classroom Learning Vs. eLearning – elearningindustry

According to the article:

“In this article, we will discuss the basic differences between eLearning and classroom learning based on 4 important factors, such as time, freedom to study a course of one’s own choice, degree of understanding, and cost-effectiveness.”

Source article:   Classroom Learning Vs. eLearning – elearningindustry.com

You might also be interested in:
GMP Training – Courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

GMP Trainer Awareness, Certification, and Master Trainer Courses

GMP Trainer Awareness, Certification, and Master Trainer Courses

This online self-study course leads participants through many different ways to teach cGMPs and QSRs. Learn what a class instructor thinks while delivering a training session to students, so you can repeat that training approach in your own organization.

How This Course Is Implemented

This course is implemented in three phases: Awareness, Certification, and Master Trainer.

  1. GMP Trainer Awareness – Students view presentations covering the course objectives below.
  2. GMP Trainer Certification – Students view the “Awareness” presentations. Students then prepare elements of a training session demonstrating the application of the content taught in the awareness course, or in some cases, capture and submit video segments of an actual or practice training session. All information submitted will be reviewed and critiqued by a team of Master Trainers. This course is taken simultaneously with the Awareness course.
  3. GMP Master Trainer – Learn GMP content to assure you know the basic GMP rules. This phase of the program is under development.

This is NOT a public seminar workshop. Our public seminar was so popular; we turned it into an online self-study course that fits into your busy schedule.

In this course, you will learn how to:

  • Apply a Participant Centered Approach to training
  • Write course objectives
  • Development a course assessment
  • Describe the difference between ice breakers and activities
  • Describe and develop ice breakers for a class
  • Describe and develop activities for a class
  • Explain the role of the instructor during activities
  • Develop an activity debriefing strategy
  • Describe various strategies for forming groups
  • Design a course presentation
  • Identify and demonstrate effective presentation skills
  • Develop stories for a class and how to deliver the story
  • Develop discussion questions
  • Develop and implement discussion follow-up strategies
  • Demonstrate the management of disruptive behavior
  • Identify the elements of a course assessment validation plan
  • Identify the elements of a course evaluation form
  • Develop a course evaluation form

Keywords:  trainer certification, train the trainer, T4T, FDA, cGMP, QSR, GMP, training

You might also be interested in:
GMP Training – Courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

Free cGMP Tip on Root Cause Analysis (RCA)

Free cGMP tip on RCA

Free GMP Tip for Root Cause Analysis

Updated April 26, 2018

You asked for it, so we delivered!

The most popular class with Allan Dewes, “Root Cause Analysis and Investigation Report Writing” is now available as an online self-study course. In 3-1/2 hours you’ll learn about the tools used to conduct a thorough deviation investigation. You’ll also learn great tips and get clear guidance on how to write a deviation investigation report. This class is not just theory and offers clear examples. Private email-based coaching is also available.

– original post follows below –

Free GMP tip on root cause analysis (RCA)

The FDA says, “Human error is not a root cause.” If your first reflex is blaming human error, it’s time to re-think the situation in order to identify the real root cause of the human error.

There are several categories of human errors: slips, lapses, and induced errors. These can account for a large percentage of errors. In order to understand these human errors in more detail, they can be investigated through the use of investigative tools such as a Walk Through Analysis or Control Barrier Analysis.

Once the underlying contributing factors and real root cause(s) are understood, then they can be controlled (in many cases).

Learn more about this topic by taking these courses by SkillsPlus Intl Inc:
Root Cause Analysis for Better Investigations – A cGMP QSR GMP Training Course
Deviation Investigation Report Writing – A GMP QSR cGMP Training Workshop

You might also be interested in:
GMP Training – Live, onsite courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

Advanced GMP Training – Root Cause Analysis & Deviation Investigation Reports

Advanced GMP Training

Advanced cGMP Training

Updated April 26, 2018

You asked for it, so we delivered!

The most popular class with Allan Dewes, “Root Cause Analysis and Investigation Report Writing” is now available as an online self-study course. In 3-1/2 hours you’ll learn about the tools used to conduct a thorough deviation investigation. You’ll also learn great tips and get clear guidance on how to write a deviation investigation report. This class is not just theory and offers clear examples. Private email-based coaching is also available.

– original post follows below –

Advanced cGMP Training – Root Cause Analysis & Deviation Investigation Report Writing

Pinpointing the wrong root cause can result in ineffective immediate, corrective, and preventive actions. Throwing fixes at the wrong things might not fix the problem. Blaming and overusing human error as the root cause can result in incomplete and ineffective root cause analysis. By taking our advanced courses, you’ll more confidently identify the real root causes, and craft clearer and more concise investigation reports.

These highly popular advanced cGMP training classes are taught at the location of your choice. You might be interested in two of our highly popular and inter-related courses.

Root Cause Analysis for Better Deviation Investigations: On-site Advanced GMP Training by SkillsPlus International Inc.

Course Objectives:

  • Use tools and techniques to effectively identify the deviation statement
  • Identify the root cause of the deviation.
  • Generate and objectively select the best corrective and preventive actions.
  • Assess the risk of implementing the corrective action and preventive action.
  • Develop a contingency plan to preventive action implementation.
  • Create corrective actions and preventive action metrics.

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

Course Objectives:

  • Increase investigation report suitability for FDA review.
  • Decrease the number of reports returned by internal reviewers.
  • Write supported deviation statements.
  • Provide a detailed background statement to include related information, investigations, affected materials and references.
  • Document deviation investigation findings.
  • State the root cause with supporting facts.
  • Generate supported, plausible, and defensible corrective actions.
  • Develop effectiveness measures for the corrective actions.
  • Generate realistic preventive actions.
  • Develop effectiveness measures for the preventive actions.
  • Develop a follow up plan for corrective and preventive actions.
  • Write accurate executive summary statements.

You might also be interested in:
GMP Training – Live, onsite courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

Introduction To FDA cGMP – A basic GMP course

cGMP basics course

Basic FDA GMP training for new hires and experienced staff.

Situation:  You’ve just hired some new employees, and your seasoned staff need refresher training.

Solution:  Contact SkillsPlus Intl Inc. for their popular basic cGMP course. It’s perfect for introducing and re-introducing essential FDA concepts to all your employees.

Call:  (415) 948-5220

Web:   Essentials for Pharmaceutical Manufacturers 

You might also be interested in:
GMP Training – Live, onsite courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website

Root Cause Analysis: cGMP Training

 

Online self-study course - Root Cause - Investigation Reports

Online self-study course – Root Cause – Investigation Reports

Updated April 26, 2018

You asked for it, so we delivered!

The most popular class with Allan Dewes, “Root Cause Analysis and Investigation Report Writing” is now available as an online course. In 3-1/2 hours you’ll learn about the tools used to conduct a thorough deviation investigation. You’ll also learn great tips and get clear guidance on how to write a deviation investigation report. This class is not just theory and offers clear examples. Private email-based coaching is also available.

– original post follows below –

GMP Training – Root Cause Analysis Workshop

One of the top reasons for a company to receive a 483 is a deficiency in the deviation investigation process. In this onsite hands-on workshop, employees learn the most effective tools to determine the real root cause of the problem. Attendees use actual plant deviations to practice the use of the tools. Allan Dewes (SkillsPlus International Inc.) has taught this course all over the world with exceptional results.

Call Allan Dewes (principal trainer):  (415) 948-5220, or
Learn more:  Root Cause Analysis For Better Investigations by SkillsPlus Intl Inc.

#FDA #QSR #cGMP #GMP #training #courses #classes #workshops

You might also be interested in:
GMP Training – Courses taught by SkillsPlus Intl Inc.


Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website