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Category: DPD

All AQAP BRC CRA DPD EN 1090/ISO 3834 EUDR Food FSC FSSC 22000 GLOBAL G.A.P. GMP+ HACCP IFS ISO 13485 ISO 14001 ISO 17025 ISO 22000 ISO 22301 ISO 22716 ISO 27001 ISO 27002 ISO 27017 ISO 27018 ISO 28000 ISO 31000 ISO 42001 ISO 45001 ISO 50001 ISO 9001 KZR NIS 2 PEFC PPWR TISAX
Counterfeit medicines in the supply chain – how does the DPD system protect patients?

Counterfeit medicines in the supply chain – how does the DPD system protect patients?

Counterfeit medicinal products are one of the most serious problems facing the modern pharmaceutical industry. A medicine lacking an active ingredient, containing it in the wrong concentration, or manufactured under uncontrolled conditions may not only fail to treat – it may kill. read more The Responsible Person in the GDP system – who is this and what are their responsibilities?

The Responsible Person in the GDP system – who is this and what are their responsibilities?

Within the Good Distribution Practice system, there is one role that cannot be delegated, replaced by a procedure or omitted from the organisational structure – the Responsible Person (RP). read more GMP in pharmaceutical transport – what requirements must a transport company meet?

GMP in pharmaceutical transport – what requirements must a transport company meet?

Transport companies serving the pharmaceutical industry operate in one of the most demanding sectors of logistics. read more Key GMP requirements – what must a pharmaceutical wholesaler comply with?

Key GMP requirements – what must a pharmaceutical wholesaler comply with?

Obtaining a licence for the wholesale distribution of medicinal products is only the beginning. read more Good Distribution Practice – what is it and who does it apply to?

Good Distribution Practice – what is it and who does it apply to?

Every medicine that reaches a pharmacy, hospital or a patient passes through a distribution chain that must meet strictly defined requirements. read more
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