Air Transport of Pharmaceutical Products


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We are proud to offer this course in a variety of training formats to suit your needs. We use the highest quality learning facilities to make sure your experience is as comfortable as possible. Our face to face calendar allows you to choose any classroom course of your choice to be delivered at any venue of your choice - offering you the ultimate in convenience and value for money.

October 2025

Date Duration Location Standard Fee Action
20 Oct - 24 Oct 5 days Half-day KES 55,000 | $ 595 Individual Group

November 2025

Date Duration Location Standard Fee Action
17 Nov - 21 Nov 5 days Half-day KES 55,000 | $ 595 Individual Group

Introduction:

The Air Transport of Pharmaceutical Products course provides participants with specialized knowledge and skills required for the safe and efficient transportation of pharmaceutical products by air. Over five days, participants will explore the unique challenges and regulatory requirements associated with the air transport of pharmaceuticals, including temperature-sensitive and high-value products. Through a combination of theoretical learning, case studies, practical exercises, and industry insights, participants will gain a comprehensive understanding of best practices, regulatory compliance, risk management, and quality assurance measures to ensure the integrity and safety of pharmaceutical products throughout the air transport process.

Duration: 5 days

Target Audience:

  • Pharmaceutical Logistics Managers
  • Air Cargo Operations Managers
  • Quality Assurance Managers
  • Regulatory Compliance Officers
  • Supply Chain Managers
  • Pharmaceutical Supply Chain Professionals

Course Level:

Course Objectives:

  • Understand the regulatory frameworks governing the air transport of pharmaceutical products, including international standards and industry guidelines.
  • Identify the unique characteristics and requirements of pharmaceutical products, including temperature sensitivity, packaging considerations, and security protocols.
  • Learn best practices for handling, storage, and transportation of pharmaceuticals to maintain product integrity and compliance with regulatory standards.
  • Develop skills in risk assessment, contingency planning, and emergency response procedures to mitigate potential risks and ensure continuity of operations.
  • Explore quality assurance measures, including Good Distribution Practices (GDP), Good Manufacturing Practices (GMP), and Quality Management Systems (QMS), to maintain product quality and compliance throughout the supply chain.
  • Gain practical experience through case studies, simulations, and site visits to pharmaceutical handling facilities and air cargo operations.

Course Outline:

Module 1: Introduction to Air Transport of Pharmaceutical Products

  • Overview of Pharmaceutical Logistics
  • Regulatory Frameworks and Guidelines
  • Characteristics of Pharmaceutical Products
  • Temperature Control Requirements

Module 2: Packaging and Handling Requirements

  • Pharmaceutical Packaging Considerations
  • Temperature-Controlled Packaging Solutions
  • Handling and Loading Procedures
  • Security and Chain of Custody

Module 3: Regulatory Compliance and Quality Assurance

  • Good Distribution Practices (GDP)
  • Good Manufacturing Practices (GMP)
  • Quality Management Systems (QMS)
  • Auditing and Compliance Monitoring

Module 4: Risk Management and Contingency Planning

  • Risk Assessment Methodologies
  • Contingency Planning for Temperature Excursions
  • Emergency Response Procedures
  • Business Continuity Planning

Module 5: Case Studies and Practical Exercises

  • Case Studies: Analysis of Real-Life Scenarios
  • Simulation Exercises: Temperature Excursion Management
  • Site Visits to Pharmaceutical Handling Facilities
  • Group Discussions and Knowledge Sharing

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Course Administration Details:

METHODOLOGY

The instructor-led trainings are delivered using a blended learning approach and comprise presentations, guided sessions of practical exercise, web-based tutorials, and group work. Our facilitators are seasoned industry experts with years of experience, working as professionals and trainers in these fields. All facilitation and course materials will be offered in English. The participants should be reasonably proficient in English.

ACCREDITATION

Upon successful completion of this training, participants will be issued an Indepth Research Institute (IRES) certificate certified by the National Industrial Training Authority (NITA).

TRAINING VENUE

The training will be held at IRES Training Centre. The course fee covers the course tuition, training materials, two break refreshments, and lunch. All participants will additionally cater to their travel expenses, visa application, insurance, and other personal expenses.

ACCOMMODATION AND AIRPORT PICKUP

Accommodation and airport pickup are arranged upon request. For reservations contact the Training Officer.

TAILOR-MADE

This training can also be customized to suit the needs of your institution upon request. You can have it delivered in our IRES Training Centre or at a convenient location. For further inquiries, please contact us on:

PAYMENT

Payment should be transferred to the IRES account through a bank on or before the start of the course. Send proof of payment to [email protected]


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