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e-Learning Good Distribution Practices (GDP) - The Entire GDP Guideline

eLearning information

Updated Tuesday, September 8, 2026 at 9:49 AM

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Understanding the GDP regulatory requirements, this e-Learning explores the GDP guideline in it's entirety.

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What’s included

  • Complete in 405–420 minutes, at your desk
  • Certificate on completion, keep for your audit trail
  • Full transcript and subtitles included
  • 365 days of access from purchase
  • Quiz-validated learning, proof you understood the material

Difficulty

Topics

GDP Packaging Manufacturing Distribution Transportation

Learning goals

  • Understanding the overarching goal of Good Distribution Practices (GDP)
  • Knowing When to Follow GDP
  • Summarize the key principles of GDP
  • And being able to locate the regulatory requirements on the internet

Why take this eLearning

  • Built by the same PCS consultants who advise real pharma firms, not generic e-learning vendors
  • A certificate you can show your QP, QA manager or auditor
  • Straightforward GMP / GDP content, no fluff, no filler
  • Closes with a quiz so you can prove you understood the material

Description

This online eLearning course on Good Distribution Practice (GDP) is a must for all persons involved in the storage, transportation, distribution, quality, or supply chain of (veterinary) medicinal products. The ultimate objective of GDP is the protection of the patient through the preservation of the quality of the medicinal product during the entire supply chain and the exclusion of fake medicines from the legal supply chain.

What are the reasons to follow this eLearning?

  • The transition from principle to practice,
  • What the course also teaches is not only the definition of GDP, but the reasons for its existence, where the legislation can be found, and the European licensing system,
  • All essential topics related to GDP are covered, including Quality Management Systems, Documentation, Facilities and Equipment, Operations, Outsourced Activities, Self-inspections, Brokers, and Transport. Particular emphasis is placed on critical processes, for example, Complaints, Returns, Suspected Falsified Medicines, and Recalls,
  • Risk-oriented and inspection-driven,
  • Questions on Quality Risk Management, Data Integrity ALCOA/ALCOA+, Chain of Custody/Chain of Control, and Temperature-Controlled Distribution can help you better comprehend regulatory requirements.

Each module contains questions, assignments, and summaries to help reinforce the learning material and is followed by a final quiz.

Upon completion of the course, participants are awarded an electronic certificate to prove their competency in GDP.

In essence, this e-learning will help you go beyond theoretical knowledge about GDP and use it effectively in your day-to-day business. This will minimize risks of non-compliance and ensure that quality medicinal products reach your patients.

NOTE: The audio is in English. Dutch subtitles are provided.

Contents

  • Introduction to the Course,
  • Basics of Medicine Distribution,
  • Quality Management System,
  • Personnel,
  • Facilities and Equipment,
  • Documentation,
  • Operations,
  • Complaints, Returns, Suspected Falsified Medicines, and Recalls,
  • Outsourced Activities,
  • Self-Inspection,
  • Brokers,
  • Quiz.

Results

Participants who successfully complete this course will receive a certificate confirming their successful completion. This certificate is digital.

Program

Lecture Description
Course Introduction
  • Start of the course
  • Content and purpose
  • GDP principles
The Basics of Distributing Medicine
GDP in a Nutshell
  • Start GDP in a nutshell
  • The goal of GDP
  • Pharmaceutical supply chain
  • Complexity
  • Main aspects of GDP
—
European Regulatory Requirements
  • Start European GDP Requirements
  • Licensing system
  • Where to find the GDP regulatory requirements?
  • Falsified Medicines Directive
  • Question
—
Assignment and summary chapter: Course Introduction
—
Quality Systems
  • What is Quality?
  • Quality System
  • What does the Quality System ensure?
Quality Management System
Management Review
  • Expected contents
  • Process
  • KPI's
  • Active Substances
—
Risk Management
  • Wat is QRM?
  • Shark Sighted Today!
  • Question
—
Assignment and summary chapter: Quality Systems
—
Personnel
—
Training Systems
  • Organogram
  • Training requirements
  • Effectivity of training
—
Personnel Responsibilities
  • Responsible Person (RP)
  • Responsible Person responsibilities
  • Delegating responsibilities
  • Designated Person (DP)
  • RP/DP difference
—
Assignment and summary chapter: Personnel
—
Premise and Equipment
  • Physical separation
  • Facility requirements
  • Temperature-sensitive products
  • Seasonal variation
  • Temperature controlled
  • Question
—
Equipment
  • Basic requirements of equipment
  • Validation v.s. qualification
  • Computerized Systems
  • Key equipment and processes
  • The V-Model
  • Question
  • Differences
—
Assignment and summary chapter: Premise and Equipment
—
Documentation
—
GDP Documents
  • Documentation structure
  • Document types
  • Records (raw data)
  • Data retention
  • Question
—
Data Integrity
  • Data
  • ALCOA
  • ALCOA+
  • Digital systems
  • Raw data?
—
Assignment and summary chapter: Documentation
—
Operations
—
Bona Fides
  • Chain of Control
  • Bona fides supplier
  • Bona fides customer
  • Returns from pharmacy
—
Storage
  • Receipt of goods / products
  • Warehouse storage
  • Question
  • Destruction of obsolete goods
—
Supply
  • Order picking and delivery
  • Question
  • Export to third countries
—
Assignment and summary chapter: Operations
—
Complaints, returns, suspected falsified medicinal products and recalls
—
Complaints
  • Regulatory expectations for complaints
  • Complaints — Complaints
  • Question
—
Returns
  • Question
  • Normal supply chain
  • Chain of custody
  • Regulatory expectations for returns
  • Saleable stock
  • Returns from pharmacies
  • Temperature-sensitive products
  • Question
Returns
Falsified Medicines
  • What is falsified?
  • Regulatory expectations for falsified medicines
  • Falsified Medicinal Directive (FMD)
  • Question
FMD
Recalls
  • Regulatory expectations for recalls
  • Recall process
  • Question
Recalls
Assignment and summary: chapter Complaints, returns, falsified medicinal products and recalls
—
Outsourced activities
Outsourced Activities
Contract giver and contract acceptor
  • Description
  • Managing outsourced activities
  • Delegation of responsibilities
—
Competence assessment
  • Assessing contractor competence
  • A new transport company
Assessing competence
Contracts
  • Delegation of responsibilities
  • Who is responsible?
  • Outsourcing of APIs
—
Assignment and summary: chapter Outsourced activities
—
Self-inspections
  • Self-inspection programme
  • Internal auditor
  • Audit process
  • Assignment
—
Assignment and summary: chapter Self-inspections
—
Transportation
  • Quality and integrity
  • Delivery
  • Outsourcing transport
  • Question
Transportation
Containers, packaging and labelling
  • Suitable containers
  • Fit for use
—
Special conditions
  • Temperature-sensitive
  • Sensitive products
  • Active Substances
  • Question
—
Assignment and summary: chapter Transportation
—
Brokers
—
Requirements for brokers
  • Quality Management System
  • Personnel
  • Documentation
  • Question
—
Summary: chapter Brokers
—
Test (Quiz / Exam)
—

Frequently Asked Questions

How long do I have to complete the eLearning?

You have 365 days from purchase to complete the course. Work at your own pace, no fixed deadlines, no live sessions to attend.

Do I get a certificate upon completing the eLearning?

Yes. Once you pass the quiz you receive a PCS Academy training certificate for the GMP or GDP topic you covered, suitable for your HR file and audit trail.

In what language are the eLearnings available?

Most courses are available in Dutch and English with subtitles. Check the course detail for the specific languages offered.

What happens after I buy an eLearning?

You receive an email with a coupon and instructions to access the course on our learning platform. For invoice or bank transfer payments, the coupon is sent once payment is received.

I did not get an email with a coupon

First check that the payment has cleared. Coupons are issued manually on working days, if nothing arrives within a few hours, get in touch and we will sort it out.

What's in an eLearning?

How the course is built

Every course is written by the same PCS consultants who advise pharma firms day-to-day. Theory is grounded in current GMP / GDP requirements and what actually works on the floor.

  • Interactive elements keep you engaged, no 60-minute talking heads.
  • Subtitles available on most courses.
  • Structured in short chapters you can pause and resume.
  • Full written transcript included for reference and audit purposes.
  • Jump back to any chapter at any time during your 365 days of access.

Learning platform

Courses are delivered through our Moodle-based platform at https://pcs-academy.site. Log in from any browser, on any device, your progress is saved between sessions.

If the platform is briefly unavailable for maintenance we will email you when it is back up.

Sharing and copyright

  • Reselling or redistributing these courses, modified or not, is not permitted.
  • Coupon codes are tied to the person or organisation on the invoice and cannot be shared.