The HRQ difference in pharmaceutical GDP training
We take the GDP guideline off the desk and turn it into a living, sustainable system in your pharmaceutical warehouses, temperature-controlled transport fleets and bonded areas, aligned with the Ministry of Health and international authorities.
Sector experts with real experience
Our trainers bring years of field experience in the pharmaceutical industry, pharmaceutical warehousing, quality assurance and GDP audits, for a high-level learning experience.
Hands-on examples and case studies
Alongside the theory, you reinforce what you learn with temperature excursion scenarios, vehicle calibration, crisis management and real audit cases.
Strong sector references
We are a trusted training partner to leading pharmaceutical manufacturers, pharmaceutical warehouses and 3PL pharmaceutical logistics providers at national and international level.
A focus on patient safety and regulation
By complying fully with EMA, FDA and TİTCK Good Distribution Practice rules, you safeguard every step from the factory gate to the patient.
Strategic gains for your business
Quality, safety and efficacy
By building GDP-compliant processes, you make sure medicines reach the end user and the patient safely, without losing stability.
Full regulatory compliance (GxP)
By learning the GDP guideline requirements of TİTCK and global health authorities, you remove the risk of penalties or quarantine in inspections.
Risk reduction and cold chain protection
You proactively analyze and prevent temperature breaks, contamination and counterfeiting risks during transport, storage and loading.
Efficiency and competitive advantage
You save costs by optimizing your operations and earn a trusted position with marketing authorization holders and buyers in the pharmaceutical sector.
Focus topics
End-to-end modular training content, from the core philosophy of GDP and cold chain management to anti-counterfeiting measures and certification audits.
- Good Distribution Practice (GDP)
- Pharmaceutical cold chain management
- Temperature mapping & climate control
- Anti-counterfeiting
- Supply chain risk analysis
- GDP audit and certification readiness
Training content
What is GDP and why does it matter?
Where Good Distribution Practice sits in the pharmaceutical sector, its legal basis (the European Medicines Agency, EMA, and the Turkish Medicines and Medical Devices Agency, TİTCK), and its critical role in protecting quality and patient safety.
Risk management in pharmaceutical logistics (QRM)
Managing the risks of transporting, storing, handling and distributing medicines with qualitative and quantitative methods.
Cold chain and temperature control
What to watch when transporting heat- and humidity-sensitive medicines (2-8°C, 15-25°C and so on), temperature mapping, data logger use and deviation management.
Documentation, traceability and record-keeping
Writing standard operating procedures (SOPs), integration with the Turkish Pharmaceutical Track and Trace System (İTS), serial and batch traceability, and data integrity.
Anti-counterfeiting and supply chain security
Security protocols to keep counterfeit, illegal or substandard medicines out of the supply chain, and supplier and customer verification steps.
GDP audits, CAPA and certification
The role of the Responsible Person (RP), running internal audits, managing CAPA (corrective and preventive action), recall exercises and preparing for GDP certification.
Who should attend?
- Managers and staff of pharmaceutical distribution and logistics companies
- Quality assurance and quality control specialists and Responsible Persons (RP)
- Supply chain, warehouse and cold chain logistics managers
- Representatives of pharmaceutical warehouses and manufacturers
- Consultants and aspiring auditors in the pharmaceutical sector
Frequently asked questions
Frequently asked questions and answers about the GDP for the Pharmaceutical Sector training.
We hold GMP. Do we also need GDP training?
GMP (good manufacturing practice) focuses on the manufacturing site and its processes. Once a medicine leaves the factory, its transport, storage and climate control on the way to pharmaceutical warehouses, hospitals and pharmacies fall under GDP. GDP is essential for a secure distribution channel.
Can you run the training in-house?
Absolutely. We can tailor the training to your warehouse areas, vehicle fleet, cold room infrastructure and specific product group (biologics, vaccines, medicines needing special climate control and so on), and run it at your company or online.
What is the role of the Responsible Person (RP) under GDP?
The Responsible Person is the authorized professional with primary responsibility for setting up and maintaining the GDP system, following up temperature deviations and handling audits. Our training also gives full guidance to RPs and aspiring RPs.