Obviousness Expert Witnesses
Obviousness expert witnesses and consultants listed here may be able to form expert opinions, draft expert witness reports, provide expert witness testimony at deposition and/or trial as or serve as consulting (non-testifying) experts on obviousness. The obviousness expert witness listings on this page are typically from fields/areas of expertise such as: Chemistry & Chemicals, Intellectual Property, Oncology, Pharmaceutical Regulation, and Pharmaceutical Research.
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Amee A Shah
Former USPTO Patent Judge - Expert Witness
BenchView Consulting LLC
Gaithersburg, Maryland
Intellectual Property
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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...
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David J Augeri, PhD
Pharmaceutical IP Litigation Expert Witness
DJ AUGERI PHARMA CONSULTING, LLC
Princeton, New Jersey
Chemistry & Chemicals, Pharmaceutical Research
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Synthetic Organic/Medicinal Chemistry, ANDA Expert Witness, DPP4 SGLT2 ANDA, HatchWaxman, Obviousness, Enablement, Infringement, Invalidity, Paragraph IV, Patent IP and Litigation, Osimertinib EGFR, GLP-1 agonists, Sitagliptin, drug discov. and development, Dapagliflozin, venclexta bcl2, btk Ibutinib, Adagrasib KRASG12C, FLT3, POSITA
With over 10 years of experience as an expert witness at DJ Augeri Pharma Consulting LLC, I specialize in pharmaceutical patent litigation, specifically in the areas of synthetic organic and medicinal chemistry, drug discovery, and CMC/API process development. I provide critical support for legal clients, offering expert reports, prior art review, claims interpretation, and testimony in U.S. and Canadian courts. My work spans patent infringement, validity, obviousness, and enablement analyses, as well as consulting on ANDA/Hatch-Waxman litigation, with a focus on diabetes and oncology drugs.
I am committed to advancing pharmaceutical innovation by combining my expertise in medicinal chemistry, structure–activity relationships, and drug development, from preclinical research to IND submissions. My technical contributions include designing alternative compounds, optimizing drug properties, and overseeing CMC facets of clinical development. I strive to provide high-quality, data-dri...
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Frederick H Hausheer, MD, FACP
Oncology Drug R & D, ICH GCP, Drug Patent Validity
HAUSHEER BIOMED, LLC USA
Austin, Texas
Oncology, Pharmaceutical Regulation
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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...