GMP Compliance Training

In cooperation with our partners, LearnAboutGMP, we now offer a full suite of GMP compliance and regulatory courses.  We offer these courses in a number of modes, ranging from self-directed online learning, to managed training where our Training Coordinator works with a group of learners through the process, to a blended learning model where we combine instructor-led training with online content, to integrated learning where online learning is backed up by on-the-job assessment of competencies. 

The current catalog of 58 courses is being added to at the rate of up to 2 new offerings per month. All courses are authored by leading, long established professionals in the sector. Full biographies of the authors are available with each course. This collection of courses is uniquely placed to help you with compliance in your business. Make sure that you have the latest information on such important topics as Data Integrity, Validation, Regulatory Compliance etc by joining our Online Community, a feature where you can see what the experts are saying about new developments.

We can also tailor Learning Paths, so learners are provided with the right courses to help them to be more effective in your regulatory compliance.

Request a FREE 14-day trial HERE.


Our courses include:

Good Laboratory Practices (cGLP)

Laboratory Data Integrity

Good Manufacturing Practices (cGMP)

Good Documentation Practices (GDocP)

Contamination Prevention and Control

Laboratory Audits

Supplier Qualification

Laboratory Investigations & Deviations

Performing Analysis in a Regulated or Accredited Laboratory

Organization and Roles

The Life Cycle of a Software Validation Protocol

21 CFR Part 11 - Introduction

 21 CFR Part 11 - Electronic Records

21 CFR Part 11 - Electronic Signatures

21 CFR Part 11 - Guidance

An Introduction to Software Validation Part 1

An Introduction to Software Validation Part 2

Corrective and Preventative Action (CAPA)

Implementing Compliant Systems in a Cloud Environment

Risk Based Equipment Qualification

Behavioural Based Quality BBQ

How to be an Effective GMP Auditor - Part 1

How to be an Effective GMP Auditor - Part 2

 How to be an Effective GMP Auditor - Part 3

IT Data Integrity in a GMP Regulated Environment

 How to Write Effective SOPs

cGMP Cases from History

 cGMP QMS Premises Personnel

cGMP Equipment Validation Complaints

 cGMP Good Practices and Quality Control

21 CFR Part 820 Subpart A – General Provisions

 21 CFR Part 820 Subpart B – Quality System Requirements

21 CFR Part 820 Subpart C – Design Controls

 21 CFR Part 820 Subpart D – Document Controls

21 CFR Part 820 Subpart E – Purchasing Controls

 21 CFR Part 820 Subpart F – Identification & Traceability

21 CFR Part 820 Subpart G – Production & Process Control

 An Introduction to Process Validation - Part 1

An Introduction to Process Validation - Part 2

 GDocP - General Rules

GDocP - Corrections

 GDocP - Logbooks

GDocP - General Test Results

 An Introduction to Cleaning Validation

Types of Contamination in a GMP Environment

 Sources of Contamination in a GMP Environment

Quality Risk Management – Contamination Prevention

 Contamination Control Strategies

The Essentials of Pharmaceutical Microbiology

 Writing a Master Validation Plan: Plain & Simple

An Easy to Understand Guide to Annex 11

 An Easy to Understand Guide to HVAC Validation

An Easy to Understand Guide to Validating Purified Water Systems

 An Easy to Understand Guide to HPLC Validation

Five Stages to Delivering Life Science Projects Successfully

 How to Perform a Failure Mode Effect Analysis (FMEA)

Principles of Statistical Process Quality Engineering

 

Contact us for further information about any of the above courses or ask for a free trial.

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