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  • Comprises newly Published Process Patents for Marketed Pharmaceutical Drugs published as CA, DE, EP, FR, GB, US and WO Patent Specifications and others as found since 1 January, 2010, at least.
  • Drug Process Patent History for specific drugs will be added on an ongoing basis, eg Atorvastatin.
  • The Database is fully Text and Structure Searchable

Pricing
Monthly Subscription: First user – £240 / month with a free trial of 1 month and a sign-up fee of £9.99 includes Quarterly Reports

Annual Subscription: First user – £1200 / year with a free trial of 1 month and a sign-up fee of £9.99 includes Quarterly Reports

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Reports comprise records taken from the Online Database. Report Types:-

  • Quarterly Reports published every quarter showing the latest records added to the database in text-searchable PDFs. Quarterly Reports have been published since 1 January 2017. 4-Weekly Reports were published from 1 January 2014 to 1 January 2017. Back issues are available.
  • Bespoke Reports from the Database using selected criteria, e.g. by Drug, Patentee etc. (contact us for prices)

 
Pricing
Annual Subscription: First user – £590 / year with a sign-up fee of £5.99

• Additional Users/Institutional Users – please contact us.

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Try the Free Quarterly Report in the Shop or preview it on the Report Sample Viewer page.

Further information

A Basic Patent Status is included in each record to briefly indicate the progress of the Patent Application. Many Process Patents do not proceed to Grant.

Due to the number of languages encountered, some countries will not be covered – however these will be included when an in-house readable language patent family equivalent emerges (eg a published EP patent specification equivalent to a CN, JP, KR etc patent specification).

Due to the prevalence of equivalent patent specifications in patent families and in an attempt to exclude repetitions, the Online Database will only include NEW patent specifications, i.e. those without previously published family equivalents. Equivalent patent family specifications may be obtained from free or commercial patent databases.

As a Marketed Pharmaceutical Drug approaches its Product Patent term expiry (including SPCs &c), numerous Process patents are filed in efforts to enhance the profitability of commercial synthesis, especially for when the Marketed Drug goes Generic. However, the FDA, for example, does not list Process Patents and these are often lost within a plethora of other pharmaceutical patents (new drugs, compositions &c) in high cost patent databases.

Database Screenshot
Adobe_PDF_iconView PDF File
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What is a Claimed Intermediate?
A Claimed Intermediate is here defined as a novel pharmaceutical process intermediate which is preferably highly stable, highly isolatable, highly purifiable (optionally with appropriate chirality) and claimed as a compound in a pharmaceutical process patent specification from which it may be subject to a 20 year patent protection term.