{"id":417,"date":"2025-07-18T13:10:41","date_gmt":"2025-07-18T12:10:41","guid":{"rendered":"https:\/\/vanrooijenconsultancy.com\/?page_id=417"},"modified":"2025-10-04T11:51:57","modified_gmt":"2025-10-04T10:51:57","slug":"gmp","status":"publish","type":"page","link":"https:\/\/vanrooijenconsultancy.com\/en\/gmp\/","title":{"rendered":"GMP"},"content":{"rendered":"
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GMP<\/h1>\n\n\n\n

Obtain your GMP licence (Manufacturer's Licence\/MIA) with expert guidance from Rooijen Consultancy.<\/h3>\n\n\n\n

Van Rooijen Consultancy assists companies in obtaining a Manufacturing Authorisation, also known as a GMP licence or Manufacturer's\/Importer's Authorisation (MIA). This licence is mandatory for companies that manufacture or import medicinal products within the European Union. We support you every step of the way, from application to inspection, ensuring that your organisation fully complies with EU GMP regulations.<\/p>\n\n\n\n

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When do you need a GMP licence?<\/h2>\n\n\n\n

Your company requires a GMP licence if you manufacture medicinal products within the European Union and\/or import medicinal products from outside the EU into the EU. A GDP licence is generally required for distribution within the EU or export outside the EU.<\/p>\n\n\n\n

How we help you obtain a GMP licence<\/h3>\n\n\n\n

Unlike certifications such as ISO, a GMP licence cannot be purchased. It is only granted by the competent government authority in the EU country where your company is based.<\/p>\n\n\n\n

We help you with<\/p>\n\n\n\n