{"id":3448,"date":"2024-03-25T21:37:16","date_gmt":"2024-03-25T20:37:16","guid":{"rendered":"https:\/\/www.heacon.de\/pharma-audits\/gdp-audit"},"modified":"2024-12-02T22:12:42","modified_gmt":"2024-12-02T21:12:42","slug":"gdp-audit","status":"publish","type":"page","link":"https:\/\/www.heacon.de\/en\/pharma-audits\/gdp-audit","title":{"rendered":"GDP audit"},"content":{"rendered":"

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Essential component of the pharmaceutical quality
system<\/h2>\n

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GDP (Good Distribution Practice), as defined in the EU guidelines, is an essential component of the pharmaceutical quality system.
\nThe GDP guidelines for finished medicinal products (EU guidelines of November 5, 2013 on good distribution practice for medicinal products for human use) have been in force since 2013 and since 2015 also for active substances (EU guidelines of March 19, 2015 on the principles of good distribution practice for active substances in medicinal products for human use).
\nThis has created a number of new requirements for audits. <\/p>\n

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The requirements of “Good Distribution Practice (GDP)” for finished medicinal products affect everything between the manufacturer and the pharmacy.
\nOur GDP audits deal with: <\/p>\n

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