Expert Witnesses for Cardiology

Found 2 experts for Cardiology

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Dr Chris Daft
Tucson, AZ
Dr. Daft provides Expert Consultation & Testimony for Patent & Trade Secret Litigation. He specializes in Medical Devices, MEMS, Signal Processing, Transducers & Microelectronics. He has participated in 14 depositions and testified at 5 trials. Details are available at https://riversonicsolutions.com/ . His expertise spans a range of technologies including wearable devices for both medical and consumer use, artificial intelligence, micro-mechanical systems, medical imaging, biometric security, and hearing aids. Dr. Daft also has experience in malpractice and product liability cases related to medical devices. A key aspect of Dr. Daft's work is his ability to simplify complex technical matters for the finder of fact, making them accessible and understandable. This skill has been recognized by courts for its effectiveness in aiding the legal process. Dr. Daft's background in patent prosecution encompasses the medical devices and artificial intelligence fields, where he has managed patent strategies for both large corporations and smaller entities. His academic achievements include publication in peer-reviewed journals and teaching engineering at the university level. His legal experience extends to involvement in Federal District Courts, International Trade Commission (ITC) section 337 investigations, and Patent Trial and Appeal Board (PTAB) proceedings. Dr. Daft provides services to plaintiffs and defendants roughly equally.
Denise Holliday
Dallas, TX
Ms. Holliday is a proven strategic innovator and tactical leader in highly regulated environments, including quality management systems, international regulatory compliance, and medical device risk management. Denise provides expertise for medical device litigation, guiding attorneys and organizations through the complexities of the global medical device industry. Manufacturers and attorneys trust Ms. Holliday to help navigate the complex regulatory landscape of medical device manufacturing and ensure compliance with standards and guidelines. Spanning more than two decades, Ms. Holliday’s career in medical device regulatory compliance and quality assurance showcases her extensive leadership experience. She conducts ISO 13485Medical Device and ISO 9001Quality Management certification audits, spearheads quality management system implementations, and manages regulatory assessments and submissions, including 510(k) and PMA.