FAQs Patent Questions

Question:How do I access sequences for a particular document?

Answer:
In order to access the sequence information for a patent or published application, you may submit the document number via the PSIPS home page. The PSIPS document detail page will then show you the number of sequences (SEQ ID NOs.) within the selected Sequence Listing. You will have the opportunity to view one or more sequences, or download the entire Sequence Listing.

Question:The laws of the U.S make no discrimination against the citizenship of the inventor, any inventor may apply

Answer:
The patent laws of the United States make no discrimination with respect to the citizenship of the inventor. Any inventor, regardless of his/her citizenship, may apply for a patent on the same basis as a U.S. citizen. There are, however, a number of particular points of special interest to applicants located in foreign countries.

Question:What is a regulatory review period determination?

Answer:
The regulatory review period is the basis for patent extension. Basically, a regulatory review period is composed of two parts: a testing phase, and an approval phase. The testing phase for a human drug product is the period between the effective date of an investigational product exemption (Investigational New Drug Application) and the initial submission of the marketing application (New Drug Application).

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