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Die Datenbank PATDPASPC enthält Informationen über ergänzende Schutzbescheinigungen in Deutschland für pharmazeutische Produkte und Pflanzenschutzmittel, einschließlich Antragstermine, Dokumentnummern,

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What is german supplementary protection certificates?

German supplementary protection certificates (SPCs) are a form of intellectual property right that extends the duration of patent protection for certain products, typically pharmaceuticals and plant protection products, by up to five years. They are intended to compensate for the lost effective patent term due to long regulatory approval processes.

Who is required to file german supplementary protection certificates?

The holder of a granted pharmaceutical or plant protection patent in Germany is eligible to file for a german supplementary protection certificate. This usually refers to the patent owner or the authorized representative.

How to fill out german supplementary protection certificates?

To fill out a german supplementary protection certificate application, the applicant must provide detailed information about their patent, the product for which the SPC is sought, the marketing authorization, and the relevant dates. It is recommended to consult with a patent attorney or intellectual property professional for assistance in completing the application.

What is the purpose of german supplementary protection certificates?

The purpose of german supplementary protection certificates is to incentivize innovation in the pharmaceutical and plant protection industries by providing extended protection for products that have undergone lengthy regulatory approval processes. They aim to compensate patent holders for the time taken to obtain marketing authorization and allow them to recoup investments made during the development and testing phases.

What information must be reported on german supplementary protection certificates?

When applying for a german supplementary protection certificate, the applicant must provide information such as the patent number, the date of grant, the product name, the marketing authorization number, the date of first marketing authorization in the European Economic Area, and the duration of the regulatory approval process.

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