Anticipation Expert Witnesses

Gaithersburg, Maryland

Intellectual Property - Administrative Patent Judge, Claim Construction, Post Grant Review, Ex Parte Appeals, PTAB, Patent Eligible Subject Matter, Patent Law, Post Grant Review, Inter Partes Review, Obviousness, Software Patents, Mechanical Devices, Patent Validity, Anticipation, Patent Law, Patents, Patent Invalidity, Indefinteness, Business Method Patents

Amee A. Shah is a former Administrative Patent Judge at the USPTO's Patent Trial and Appeal Board (PTAB), bringing nearly a decade on the bench and over 30 years of combined legal, technical, and patent expertise to her expert witness and litigation support practice. As an APJ, Judge Shah presided over and authored decisions in inter partes review (IPR) proceedings and ex parte appeals across all five PTAB technology areas — business methods, mechanical, electrical, biotechnology, and chemical — spanning technologies including data processing, graphical user interfaces, artificial intelligence, mechanical structures, computer systems, semiconductors, and medical devices. She also served as a PTAB point of contact for patent eligible subject matter under 35 U.S.C. § 101, reviewing and authoring decisions designated as informative guidance and training examiners on USPTO § 101 guidance implementation. Before joining the bench, Judge Shah spent over a decade as a USPTO Primary Examin...

Austin, Texas

Oncology, Pharmaceutical Regulation - Oncology Drug Development, Patent Validity, ICH GCP, Written description, Enablement, Obviousness, Anticipation, Pharmacology, FDA, EMA, NMPA/China, PMDA/Japan, Drug formulation, Medical Safety, Phase 1-3 Clinical Trials, Drug Product Safety, Medical Oncology, Breach of Contract - Pharma/Biotech, Commercially Reasonable Efforts, Damages

Dr. Frederick (Fred) Hausheer is a physician-scientist with over 37 years of executive leadership and management experience in US and international (EU, JP, China, others) commercial pharmaceutical research and development (Phase I-III), preclinical translational and clinical medicine, clinical pharmacology, ICH GCP compliance and commercial development strategy and risk management of novel cancer therapeutics. His commercial research and development experience includes cytotoxic agents, targeted agents, immuno-oncology therapeutics, cell therapies (BMT, CAR-T), and supportive care medicines. He is an inventor/co-inventor on more than 400 issued United States and international pharmaceutical patents, and author/co-author of more than 200 scientific/medical publications. He is an experienced former CEO and Chief Medical Officer with several biopharma companies and a former NCI-Designated Clinical Investigator, NCI-Institutional Review Board voting member, and NCI-Experimental Ther...