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Therapeutic Innovation & Regulatory Science
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July 5, 2018
Validation Master Plans: Progress of Implementation in the Pharmaceutical Industry
Clare Elser, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
June 10, 2024
EU's Medical Device Expert Panels: Analysis of Membership and Published Clinical Evaluation Consultation Procedure (CECP) Results
Colleen Watson, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 19, 2018
Incentivizing Quality in the Manufacture of Pharmaceuticals: Industry Views on Quality Metrics and Ratings
Cesar Medina, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 22, 2018
The Role of Universities in the Commercialization of Medical Products: A Survey of Industry Views
Michael W Jamieson, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 18, 2018
Global Regulatory Dissonance: A Case Study of Industry Views on the Development of Drugs for Postmenopausal Osteoporosis
Neal E Storm, Frances J Richmond
Therapeutic 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 Church
Biopreservation and Biobanking
|
April 25, 2019
Biobank Continuity Management: A Survey of Biobank Professionals
Terry David Church, Frances J Richmond
Frontiers in Robotics and AI
|
October 18, 2021
Turning Neural Prosthetics Into Viable Products
Gerald E Loeb, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 18, 2018
Management of Clinical Trial Agreements: Current Practices of Investigators in the United States
JoAnn P Pfeiffer, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
May 31, 2024
Standalone Regulatory Agreements for Product-Development Collaborations in the Medical Products Industry
Mary E Wilhelm, Nancy Pire-Smerkanich, Frances J Richmond
Page
of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Therapeutic Innovation & Regulatory Science
|
July 5, 2018
Validation Master Plans: Progress of Implementation in the Pharmaceutical Industry
Clare Elser, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
June 10, 2024
EU's Medical Device Expert Panels: Analysis of Membership and Published Clinical Evaluation Consultation Procedure (CECP) Results
Colleen Watson, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 19, 2018
Incentivizing Quality in the Manufacture of Pharmaceuticals: Industry Views on Quality Metrics and Ratings
Cesar Medina, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 22, 2018
The Role of Universities in the Commercialization of Medical Products: A Survey of Industry Views
Michael W Jamieson, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 18, 2018
Global Regulatory Dissonance: A Case Study of Industry Views on the Development of Drugs for Postmenopausal Osteoporosis
Neal E Storm, Frances J Richmond
Therapeutic 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 Church
Biopreservation and Biobanking
|
April 25, 2019
Biobank Continuity Management: A Survey of Biobank Professionals
Terry David Church, Frances J Richmond
Frontiers in Robotics and AI
|
October 18, 2021
Turning Neural Prosthetics Into Viable Products
Gerald E Loeb, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
September 18, 2018
Management of Clinical Trial Agreements: Current Practices of Investigators in the United States
JoAnn P Pfeiffer, Frances J Richmond
Therapeutic Innovation & Regulatory Science
|
May 31, 2024
Standalone Regulatory Agreements for Product-Development Collaborations in the Medical Products Industry
Mary E Wilhelm, Nancy Pire-Smerkanich, Frances J Richmond
Page
of 2