Good Distribution Practice (GDP)
This is a new programme designed specifically for staff working in the Pharmaceutical Wholesale and Distribution Industry. It will assist them in understanding and applying Good Distribution Practice principles to practical workplace situations.

The development of the rules and guidelines of GDP will be discussed with the delegates, who will then go on to investigate the implications, potential risks to product safety and the control systems in place within their organisation. The loop will be closed by relating these findings back to the organisation's quality system.

The course concludes with a case study to allow the delegates to put their learning into practice.
J E M O Limited
Established since 1984
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Pharmaceutical Internal Auditor Training
Good Distribution Practice (GDP)
Pharmaceutical Auditor/lead auditor Training
Pharmaceutical Course
GMP For Pharmaceutical Packaging Awareness Workshop
Who should attend?
The course has been designed to be interesting and engaging to operators, but is appropriate to all levels within the organisation that might have an impact on product quality.
More information and get a quote
“It opened my eyes to what professional supplier auditing is about”

“Superb explanation of the PS 9000 series of GMP standards and how to audit against them”

“Fulfilled my requirements completely”

“Illustrated throughout with pharmaceutical industry examples”

All of our courses can be customerised to your needs normally with no extra cost.  Please feel free to contact us for more details and/or request a competitive quote.  Contact us on phone +44 (0) 1249 44 75 44 or complete our Enquiry form
Copyright © J E M O Ltd 2017 All Rights Reserved
J E M O Ltd Registered in England & Wales Reg. no 4933247
PS...Britain's best kept secret
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Hot off the press
PS 9000: 2011
Download the latest PS9000:2011 standard from PQG for free
Medical Device Auditing to ISO 13485
Key Subject Areas


• Documentation

• Premises and Equipment

Course Objectives

The objectives of the course are that delegates will:

'Close the loop' by linking regulatory requirements to Quality Procedures (ISO 9001) and everyday working practices.

CQI Introduces a new Grade
• Transportation
• Returns and Recalls

• Self Inspection (Internal audits)
Introduction to latest PS9000:2011
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Auditor Training, Assessment & Consultancy
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ISO 9001:2015 Gap Analysis
Auditing & Implementation Tools