Good Distribution Practice for Veterinary Medicinal Products: (EU) 2021/1248

5/5
141
Good Distribution Practice  Veterinary Medicinal Products

Duration :

1

1 hour(s)

Skill level:

Regulatory

Language:

English

Final exam:

Yes

Certificate of Completion:

Yes

CEU / CPD Accreditation:

Yes

Certification:

Successful completion provides learners with a dated, traceable and downloadable certificate for the course : 

Each certificate is CPD/CEU accredited and 21 CFR PART 11 compliant. Certificates validity can be checked online through our certificate online checker. They can also be shared on Linkedin.

Description:

The quality, safety, and efficacy of veterinary medicinal products depend not only on how they are manufactured but also on how they are stored, handled, and distributed. Any lapse in the distribution chain can compromise product integrity, potentially affecting both animal and public health.

This course focuses on maintaining the quality and integrity of veterinary medicinal products throughout the entire supply chain, as required by Commission Implementing Regulation (EU) 2021/1248.

Learners will gain a clear understanding of the essential elements of Good Distribution Practice (GDP) and the EU regulations that ensure veterinary medicines are stored and distributed safely.

Who should enroll?
This course is designed for professionals involved in the storage, handling, and distribution of veterinary medicinal products across the supply chain. It is particularly valuable for:

  • Quality Assurance and Quality Control professionals
  • Warehouse and Distribution Managers
  • Logistics and Supply Chain professionals
  • Wholesalers, Importers, and Distributors of veterinary medicines
  • Veterinary hospital staff involved in product storage or transport

 

What you’ll learn?

  • Interpret and apply the requirements of Commission Implementing Regulation (EU) 2021/1248
  • Ensure that storage facilities, equipment, and transport conditions protect the quality and integrity of veterinary products
  • Implement compliant documentation and record-keeping practices
  • Prepare your organization for regulatory inspections and audits focused on veterinary medicinal products

By the end of the course, learners will be equipped with the knowledge and tools to apply GDP requirements effectively within their organization. Upon successful completion, you’ll receive a validated certificate accredited with CPD/CEU credits and recognized by auditors.

 

Curriculum

 

Introduction

Lesson 1: General Provisions

Lesson 2: Building a Quality Management System in GDP

Lesson 3: Personnel Roles and Responsibilities

Lesson 4: GDP Compliance of Premises and Equipment

Lesson 5: Documentation and Record Keeping

Lesson 6: Operations

Lesson 7: Complaints, Returns, Suspected Falsified Medicinal Products and Medicinal Product Recalls

Lesson 8: Outsourced Activities

Lesson 9: Self-Inspections

Lesson 10: Transport

Lesson 11: Final Provisions

Conclusion

Glossary

Quiz

Author:

khurram
Khurram Rehman
Kuhman has a M.Sc. degree Industrial Pharmaceutical Sciences, School of Pharmacy, University of Manchester. Thanks to 25 years of experience he a recognized expert in GMP (batch release, quality management, auditing, regulatory affairs, production, quality control) and GDP environment (distribution, cold chain, temperature mapping, quality management). He took part in 150+ GDP and quality system audits .

Reviews:

5/5
141

$95

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This course includes:
One-year access
Updated content every month
Certificate of completion

GxP-Training Benefits

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$95.00 / year

$95.00 / year

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