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GMP:KnowHow Pharma Logistics (GDP) | Free Demo Access

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  • You will receive your login credentials via email. 
  • Throughout the week, you will receive further information about the GMP:KnowHow Pharma Logistics (GDP) directly in your inbox. 
  • Customer support is available to assist you at any time. 
  • You can also direct questions about the content to the editorial team and receive personalized responses. 
  • You do not need to cancel your demo access. The free access will end automatically. 

Advantages at a glance

How the GMP:KnowHow Pharma Logistics (GDP) supports you

The supply chain for medicinal products and medical devices is international in scope and involves many participants. Understanding of GDP varies greatly depending on the country and industry. Various guidelines and laws must be taken into account, as well as the interfaces with GMP.

To ensure patient safety, the supply chain for medicinal products and medical devices is subject to strict regulation and monitoring. In Europe, the EU GDP Guidelines are the leading document.

Here you will find expert knowledge from practice, requirements from the perspective of the authorities, application examples and sample documents.

  • Quality Management
  • Personnel
  • Premises and Equipment
  • Documentation
  • Operations
  • Complaints and Returns
  • Outsources Activities
  • Self-Inspections
  • Transportation
  • EU GDP Guidelines (2013/C 343/01 and 2015/C 95/01)
  • EU GMP Guide Part I – III and Annexes
  • AMG, AM-HandelsV, AMWHV
  • MPDG, HMG, AMBV
  • PIC/S (PE 011-1, PI 047-1 Annex)
  • WHO (GSDP & GTDP)
  • DIN EN ISO 9001:2015, 13485:2016

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Yannic Matt, Kundenbetreuung und IT-Support beim GMP-Verlag

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