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Medical Device Reporting Regulation Experts| The following experts are available as Medical Device Reporting regulation consultants and Medical Device Reporting regulation expert witnesses. Intota experts are peer-recommended authorities who have been carefully selected and rigorously screened. | |
| | Definition: Medical Device Reporting Regulation -
A regulation established in 21CFR 803.24 that mandates procedures and obligations for medical device manufacturers to report to the FDA adverse effects, serious injury, and malfunctions that meet certain criteria. (A law establishing obligations for users and distributors to report similar adverse events was enacted in 1992.) Synonyms: MDR code, MDR law, MDR ordinance, MDR regulation, MDR rule, MDR statute, Medical Device Reporting code, Medical Device Reporting law, Medical Device Reporting ordinance, Medical Device Reporting rule, Medical Device Reporting statute |
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| |  | | Expert in Electrical and Biomedical Engineering, Patent Analysis
Expert is an expert in medical implants, devices and instrumentation; electrical and biomedical engineering; hospital x-ray and power systems; electrical power systems; electrical fire investigation; product safety and design deficiencies; ... See full profile | | Illinois (IL), USA  | | | |  | | Expert in Healthcare Information Technology, Biomedical Device Integration, Clinical Informatics
Expert has more than 10 years experience developing and working with electronic medical record software, including developing healthcare information technology products (medical surgical, critical care) in the form of clinical information and ... See full profile | | Maryland (MD), USA | | | |  | | Expert in Clinical Trials, Drug Development, Medical Monitoring, AIDS, FDA Regulation, Safety Assessment
Expert is a public health professional who has extensive international and domestic experience. She has worked for pharmaceutical/biotech companies, hospitals, public health institutions, non-profit organizations, in the areas of clinical trials ... See full profile | | California (CA), USA | | | |  | | Expert in Medical Device Research and Development
Expert has over 30 years experience in medical device design dealing with all phases of design -- brainstorming, concept design, proof of concept testing, prototyping, cost / task estimating, project planning, project management, detailed design, ... See full profile | | Minnesota (MN), USA | | | |  | | Expert in Healthcare Consulting: Strategic Planning, Product Development, and Product Launch
Expert has been providing expert strategic and operational advisory services to healthcare investors and development stage healthcare companies for nearly 10 years. He has been involved in direct healthcare management for over 15 years, and ... See full profile | | Massachusetts (MA), USA | | | |  | | Expert in General Management; Finance, Accounting, Sales, Marketing, IT, Manufacturing, Strategic Planning
Expert has extensive hands on experience in all aspects of accounting. He has established activity based cost systems and selected and implemented various accounting software applications, such as Peachtree and Oracle ERP. See full profile | | Wyoming (WY), USA | | | |  | | Expert in Wound Care Technical Product Development and Commercialization
Medical product development. Expert has expertise in developing and commercializing wound care products. His experience has included observing existing wound care techniques, devising new products that work as a system to improve existing ... See full profile | | Pennsylvania (PA), USA | | | |  | | Expert in Medical Products Packaging: FDA Package Validation, Development Standards, Test Methods, ISO 11607
Expert has expertise in the field of medical device packaging for both single use disposable devices and for long-term implantable medical devices. His primary involvement has been in the design, development, and qualification of device ... See full profile | | Minnesota (MN), USA | | | |  | | Expert in FDA Regulatory Consultant for Medical Devices, Cosmetics, and OTC Drugs
Expert is a renowned authority in the cosmetic, OTC drug and medical device industries. He has had over 40 years of experience dealing with regulatory, scientific, and technical issues for FDA regulated industries. He served as Senior Vice ... See full profile | | Maryland (MD), USA | | | |  | | Expert in Pharmaceutical Development & Validation
Expert has over 20 years of broad-based experience with pharmaceutical product development. His work in this area has ranged from early phase 1 drug characterization to phase 4 market product launch and validation. See full profile | | Pennsylvania (PA), USA | | | |  | | Expert in FDA Compliance, Pharmaceutical New Products, Management Training, Seminars, Inspections, Audits
During his employment with the Food and Drug Administration, Expert received five grade promotions, with his last position being that of Director of the Science Branch of the Philadelphia District. Expert's area of responsibility included all the ... See full profile | | Georgia (GA), USA | | | |  | | Expert in Medical Device Product Development
Expert has designed, invented, and developed a wide range of single-use medical devices, including wound dressings, absorbent-hygienic products, compression garments, first aid products, and drapes and gowns. See full profile | | North Carolina (NC), USA | | | |  | | Expert in Sterilization, Sterilizers
Sterilization; sterilizer; autoclave. Expert has over twenty years of experience in the design, production, and marketing of steam and gas sterilization equipment. His experience has covered small table top sterilizers through ... See full profile | | North Carolina (NC), USA | | | |  | | Expert in Biomedical Engineering; Medical Devices
Ip Projects Catheter stabilizing device Dental Instrument Implant Seeds Intrauterine pressure catheter Vascular Catheters (3) Over 30 years experience in medical product design and development experiences in Anesthesiology, Assistive Technology, ... See full profile | | Illinois (IL), USA | | |  |
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