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Expert ID: 724357 New Hampshire, USA

Expert in Medical Device Product Development; Machine Design; Biomedical Engineering

Medical device product development engineer. He performed research on adding an antimicrobial agent to a silicone rubber medical device molded using LIM. Research included materials, methods of molding, color changes, and effect to biocompatibility. His library contains many materials available…

Expert ID: 728303 California, USA

Expert in Medical Devices; Product Development, Manufacturing, Marketing, Business Practices, Intellectual Property, Commercial Contracts, Corporate Finance, M&A

Expert has been the CEO or chairman of seven medical device companies in four countries - four public, three private, and has been a member of the Board of Directors of 10 companies. He is an expert in areas of…

Expert ID: 727864 Maryland, USA

Expert in Product Development and Manufacturing Technology Transfer in Composite Materials for Industrial, Biotech and Medical Devices

Expert's principal expertise lies in conducting original research, development and evaluation of alternative process capabilities, in support of new product development. His work has typically led to the establishment of new manufacturing platforms for a variety of material science-oriented businesses…

Expert ID: 726016 New Jersey, USA

Expert in Biotech, Pharma and Medical Device Product and Process Development, Scale-up & Commercialization

His approach to process validation is that PV begins at the process development phase. A process that is well understood, well defined as per the critical to quality attributes with an understanding of the variable interactions prior to the definition…

Expert ID: 725382 Tennessee, USA

Expert in Biomedical Engineering, Patents, Medical Device Design, Product Development, Eye Activity Devices,

He has served as a consultant as well as trained and led numbers of team consultants in application software development projects for over 20 years. Masters Degree specializes in optics and diagnostic/remediative processes and devices based on eye activity. PhD…

Expert ID: 723802 Canada

Expert in Medical Device Business Development, Strategic Planning, Due Diligence, and Product Development

Expert has a doctorate in Biomedical Engineering and remains current with many of the advances in this field. He currently sits on the grant selection committee for the National Research Council of Canada. He has performed numerous consulting assignments within…

Expert ID: 722270 United Kingdom

Expert in Pharmaceutical Product Development, Drug & Medical Device Safety, Regulatory Affairs

Expert is active in U.K. General Practice with wide therapeutic area knowledge and practical patient prescribing. He has a good understanding of the U.K. health system, formulary adoption, N.I.C.E., and reimbursement. Expert has 15 years of experience in the design,…

Expert ID: 736630 Illinois, USA

Expert in Cybersecurity Strategy, Roadmap Development, Cloud: Migration, Standards Dev, End-to-End Process Development, Go-Live Strategy after Workload Migration, Product Cybersecurity Functions

Summary • Results driven Cyber security and Risk Management professional with 24+ years in regulated industries. • Strong background leading cross-functional, global organizations in Cyber Security, Privacy, Risk Management, Audit and Data Protection functions • Specialist and Subject Matter Expert…

Expert ID: 723693 Florida, USA

Expert in Pharmaceutical Science; Preformulation, Development, Chemistry, Manufacturing & Control (CMC) Issues; Paragraph IV Hatch-Waxman & Canadian Notice of Allegation

As the development of a pharmaceutical reaches Phase 3, prior to submission of an NDA, method validation is required. Validation is a demonstration of optimization. By demonstrating the capacity of a method within the bounds of validation, optimal conditions for…

Expert ID: 721780 New Jersey, USA

Expert in Biocompatibility Testing and Biomaterials for Medical Devices

Consulting experience in the set up and protocols for biological tests, pre-clinical evaluation submission summaries (regulatory), product (medical device) cleaning validation, GLP laboratory set up and management, biocompatibility/ toxicilty testing Strategy for the pre-clinical evaluation / toxicity testing of an…

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