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About
Good Distribution Practice (GDP) for Drivers ensures that medicinal products are transported safely, securely, and under appropriate conditions throughout the supply chain. It focuses on maintaining product quality and integrity during transit, while ensuring compliance with regulatory expectations under EU and UK GDP guidelines.
This Good Distribution Practice: Adapted for Drivers (English) Course & Certification provides essential training for drivers involved in the transport of pharmaceutical products. The course covers legal requirements, responsibilities, safe handling practices, temperature control, documentation, delivery procedures, handling of incidents, counterfeit awareness, product recalls, and inspection readiness. Upon completion, learners receive a certification demonstrating their understanding of GDP principles specific to transportation and delivery roles.
- Pharmaceutical Delivery Drivers and Couriers
- Logistics and Transport Personnel in Pharma Supply Chains
- Warehouse Dispatch and Distribution Staff
- Cold Chain Transport Drivers
- Third-Party Logistics (3PL) Drivers handling medicinal products
- Pharmacy and Healthcare Delivery Staff
- Anyone responsible for transporting medicinal products
- Entry-level professionals seeking GDP driver certification
What you will learn
Understand pharmaceutical distribution regulations, GDP principles, and the legal requirements governing medicinal product supply chains.
Learn the roles and responsibilities of management, responsible persons, and warehousing and distribution personnel.
Develop knowledge of storage conditions, environmental control, transportation practices, documentation, and SOP requirements in pharmaceutical distribution.
Gain understanding of product recalls, counterfeit medicinal products, self-inspections, and compliance procedures to maintain product quality and patient safety.
Course Syllabus
- Rationale & Development
- UK and EU Legislation
- Provision of Information to Authorities
- Management and Licence Holders
- What Is a Responsible Person?
- Warehousing and Distribution Personnel
- Facilities and Equipment – General
- Receipt of Deliveries
- Expectations of Storage Facilities
- Environmental Control
- Cold Storage
- Sales Orders
- Authorised Supply
- Standard Operating Procedures (SOPs)
- What Should SOPs Cover?
- Performance Checking
- Training Records
- Other Records
- Key Points About Documentation
- Principles of Transportation
- What Does This Mean in Practice?
- Is the Transportation Suitable?
- Deliveries
- What About Goods with Special Requirements?
- What If Something Goes Wrong?
- Complaints and Returns
- Returns of Non-Defective Medicinal Products
- Key Points About Distribution
- Practicalities
- Classes of Product Recall
- Recall Procedure
- Destruction
- Training
- The EU Falsified Medicines Directive (FMD)
- US Drug Quality and Security Act
- What Should You Do If You Find or Suspect That Products Are Fakes?
- Who Should Carry Them Out?
- What Should Self-Inspection Achieve?
- Preparing for Inspection
- References and Links
Course Benefits
Gain Continuing Professional Development (CPD) Points, accredited by The Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom. These can be used to count towards the distance learning element of any scheme that comes under the umbrella of The Academy of Medical Royal Colleges or any other scheme for which there is mutual recognition.
Receive a personal certificate to show your subject knowledge on course completion.
You get excellent value through our cost-effective prices. We can also offer you group discounts on larger purchases.
The course saves you time through the convenience of online availability. This lets you complete the interactive course at your own comfort.
You will stay up to date with any legislative changes in GDP as our training courses are constantly monitored, reviewed and updated.
The course content has been developed to ensure that you comply with GDP legislation through the application of learning outcomes. The course is written by Louise Handy, who is a past chairperson of the Research Quality Association (RQA






