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Collection of GMP's for pharmaceutical production
The GMP Handbook for pharmaceuticals
Quality Systems Handbook for MedDev
GMP translations (FR, IT, SE, DK)
Search tool and document library. Find you way in regulations, guides and other reference documents.
Medicinal/Pharmaceutical industry; storage and distribution of pharmaceutical products including raw materials (excipients and APIs), intermediates and final dosage forms.
This course is designed specifically for staff working in wholesale and distribution of medicines. 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 organization. By relating these findings back to the organization’s quality system, the delegates discover how quality is an integral part of their business.
The course includes a number of workshops and case studies to allow the delegates to put their learning into practice.
Regulations and guidance
The Quality System
Risk management
The responsible person
Self inspection
The inspection process
Facility management
Stock management
Temperature control and monitoring
Transport – including Cold Chain
Counterfeit medicinal products
The objectives of the course are that delegates will understand the regulatory requirements and constraints facing wholesalers and distributors of medicinal products. The attendees will become familiar with the relevant sections and clauses of the EU Rules, as well as being able to develop their organization’s process and identify the controls necessary to ensure compliance with GMP/GDP regulations and guidelines and, at the same time, operate effectively in a competitive market.
The course is aimed at anyone who has responsibility for finished pharmaceutical products, intermediates or raw materials during storage and distribution – including transportation. This will include staff working in Quality, Operations, Transportation etc.
The course includes a significant number of practical exercises, case-studies and workshops to allow delegates to investigate real situations and develop practical solutions.
Delegates will be encouraged to share personal experiences and solutions to the various challenges faced in everyday work.
Course No:5222 |
Instructors: |
Next course:December 8-9, 2010, Copenhagen, Denmark |
Course venue: |
Agenda:Day 1: 10.30-17.00 (Registration 10.00-10.30) |
Price:€ 1195 incl. course material, lunches and refreshments |
Discounts:We do not offer any general discounts. Instead we will always offer best value courses for good value fees to ALL our attendees. For larger groups we can offer discounts based on case by case discussions, please contact for quotation. We do not offer or practise any general company discounts without commitments and/or written agreements. |
Cancellation policy:Registration is binding and when you have received our confirmation the following conditions are know and accepted. If you for any reason is unable to attend, substitution is always possible and preferred. All cancellations and/or substitutions must have been communicated with and confirmed by us. Cancellations received less than 21 calendar days before course start are subjected to a service charge of 200 € (Euro). Cancellations received less than 7 calendar days prior the course, or failure to cancel or "no-show", will be charged in full. Courses may be cancelled by the organizer if bookings fail to reach minimum numbers, and in such circumstances course fees will be refunded, or granted to attend another course for the same value. We are not responsible or liable to any costs in conjunction with a cancelled course. Under normal conditions a cancellation decision is taken +6 weeks prior the course start. |