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Therapeutic Innovation & Regulatory Science|June 10, 2024
EU's Medical Device Expert Panels: Analysis of Membership and Published Clinical Evaluation Consultation Procedure (CECP) ResultsColleen Watson, Frances J RichmondTherapeutic Innovation & Regulatory Science|July 5, 2018
Validation Master Plans: Progress of Implementation in the Pharmaceutical IndustryClare Elser, Frances J RichmondTherapeutic Innovation & Regulatory Science|September 19, 2018
Incentivizing Quality in the Manufacture of Pharmaceuticals: Industry Views on Quality Metrics and RatingsCesar Medina, Frances J RichmondTherapeutic Innovation & Regulatory Science|September 22, 2018
The Role of Universities in the Commercialization of Medical Products: A Survey of Industry ViewsMichael W Jamieson, Frances J RichmondTherapeutic Innovation & Regulatory Science|September 18, 2018
Global Regulatory Dissonance: A Case Study of Industry Views on the Development of Drugs for Postmenopausal OsteoporosisNeal E Storm, Frances J RichmondTherapeutic Innovation & Regulatory Science|January 12, 2020
Graduate Training Capacity for Regulatory Professionals at US Universities: Are We Facing a Talent Crisis?Frances J Richmond, Terry D ChurchBiopreservation and Biobanking|April 25, 2019
Biobank Continuity Management: A Survey of Biobank ProfessionalsTerry David Church, Frances J RichmondFrontiers in Robotics and AI|October 18, 2021
Turning Neural Prosthetics Into Viable ProductsGerald E Loeb, Frances J RichmondTherapeutic Innovation & Regulatory Science|September 18, 2018
Management of Clinical Trial Agreements: Current Practices of Investigators in the United StatesJoAnn P Pfeiffer, Frances J RichmondTherapeutic Innovation & Regulatory Science|May 31, 2024
Standalone Regulatory Agreements for Product-Development Collaborations in the Medical Products IndustryMary E Wilhelm, Nancy Pire-Smerkanich, Frances J RichmondPageof 2