Good Distribution Practice

Course Essentials

  • Duration

    1 Day
  • Price

    £650.00 ex.VAT
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Learn about GDP and how it is applied during warehousing and transportation of pharmaceutical products.

Course Overview

Delegates will learn about GDP and how it is applied during warehousing and transportation of pharmaceutical products. Delegates will leave the course with a clear understanding of the requirements of EU GDP and how it is used.

Who will the course benefit?

This GDP course is aimed principally at personnel new to working with GDP as well as those needing an update on more recent changes in GDP requirements and expectations. The course is also of great value to anyone who is, or wishes to be, a Responsible Person (RP). In addition the course will provide those used to working with Good Manufacturing Practice (GMP) an insight into the principle similarities and differences between GDP and GMP.

Course Content:

  • An introduction to GDP
  • The similarities and differences between GMP and GDP
  • Why do we have GMP and GDP in pharmaceuticals?
  • Licences for medicines and enforcement
  • The legal status of GDP
  • The structure of the EU Guide to GDP
  • Current and future issues in GMP
  • The Falsified Medicines Directive (an overview)
  • Duties of Management and the Responsible Person
  • The principle GMP requirements for documentation and records
  • GDP in the warehouse
  • GDP during transportation
  • The recall mechanism

Course Tutor:

Dominic Parry has worked in the pharmaceutical industry since 1992, and is a leading pharmaceutical quality management specialist. He worked for 4 years at Evans Medical Limited (now Novartis Vaccines) as a Production Development Scientist. He then moved to Hoechst Marion Roussel (now Patheon, UK), where he worked for 4 years as a Quality Assurance Officer and then Validation Manager for the sterile manufacturing operations. Over the past 15 years he has worked as a leading pharmaceutical GMP trainer and Quality Management System specialist. He works closely with pharmaceutical companies and their suppliers on evaluating, developing and continually improving their quality systems. He is generally recognised as one of the leading GMP trainers in the UK and brings an enormous amount of interest, enthusiasm and fun into the training he presents. He is Managing Director of Inspired Pharma Training Ltd.

Course Location:

UK courses (Reading, Berkshire)
The Holiday Inn – Reading South, 500 Basingstoke Road, Reading, Berkshire, RG2 0SL, UK. The hotel is very close to Junction 11 of the M4 – 25 miles west of London’s Heathrow Airport.
Telephone: + 44 (0)871 942 9067
e-mail: reservations-reading@ihg.com
Web: http://www.hireadingsouthhotel.co.uk

Course Cost: £650.00 per delegate plus VAT. Course will be charged in GB pounds.

VAT will not be charged for courses held outside the UK. VAT will be charged for the courses held in the UK, however delegates from outside the UK but within the European Union (EU) will not be charged VAT if they supply their own company’s national VAT number when booking. VAT will not be charged for any delegates coming from outside the EU.

The cost includes:

  • Refreshments and lunch during the course times.
  • Course folder containing copies of slides and supplementary notes and handouts.
  • Course attendance certificate.
  • Full tutor support and access during course times.

The cost of accommodation is not included in the course cost. If required you should book accommodation yourself directly with the hotel.

Payment can be made by cheque, electronic transfer, credit or debit card. Payment must be made before the course start date. Either payment or a Purchase Order number will be required to secure a place on the course. We accept VISA, MASTERCARD and AMEX. Credit card transactions are subject to a 1.5% handling fee.

To book your place:

Please email to reserve a place or call +44 1635 866699 quoting "Clarity Compliance".

Get in touch

Discover how we can help your organisation.

+44 (0)1633 400939

+44 (0)7735 204233

Why Choose Clarity?

Our Philosophy

Our philosophy is to treat validation of all pharmaceutical systems as a lifecycle process requiring monitoring from cradle to grave to ensure control of the system.

Our Audit Services

Our audit services are a key component of this lifecycle approach comprising in a unique set of tools designed to ensure compliance is effectively evaluated, managed and maintained.

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