The USPTO has announced the COVID-19 Prioritized Examination Pilot Program to incentivize prompt research into treatment of this pandemic. The program will benefit small and micro entities by allowing them to file for prioritized examination without the typical fees. To qualify for this program, the claims of the application must cover a product or process that is subject to FDA approval for use in the prevention and/or treatment of COVID-19. The USPTO aims to reach final disposition of applications to this program within six months, if the applicant responds promptly to USPTO communications. WHIPgroup attorneys have significant experience in products and processes subject to FDA approval, including medical devices and chemical compositions. We are ready and able to help you take advantage of this program.
By Robert D. Keeler and Lauren C. Matturri California’s online data protection law, the first U.S. law of its kind to protect online data privacy, will begin to be enforced on July 1, 2020. The [Read More…]
How do you market something over the Internet that is secret for much of its life? This question has confronted business owners and inventors for years. Monetizing intellectual property can be labor intensive, high cost [Read More…]
By Christopher J. Stankus COVID-19 has brought numerous changes to the legal industry’s approach to working remotely. Some changes have been ordered by the courts, while others have been instituted by practitioners. Some of these [Read More…]