Search
shelleyamaves
Oct 13, 20232 min read
Presentations, Tutorials and Resources
Biologics FDA Regulatory Overview - Video BioPhia Consultant Ed Moore presents a training video as part of the Great Lakes Medical...
13 views0 comments
shelleyamaves
Oct 13, 20231 min read
BioPhia Now Offers Complete Package for Toxicological Risk Assessments
BioPhia Consulting is pleased to announce the licensing of Lhasa Limited’s Derek Nexus and Sarah Nexus software offering BioPhia clients...
12 views0 comments
shelleyamaves
Sep 30, 20232 min read
Resources and Presentations
Complement Activation in Excorporeal Therapies Richard Johnson PhD The committee Roundtable on Biomedical Engineering Materials and ...
6 views0 comments
shelleyamaves
May 11, 20231 min read
Regulatory Path for Artificial Intelligence / Machine Learning (Software as a Medical Device (SaMD))
BioPhia Consultant Ed Moore presents a training video as part of the Great Lakes Medical Jumpstart I-CORPS program discussing the...
26 views0 comments
shelleyamaves
Jun 11, 20221 min read
The Impact of the FDA on Product Development
The following presentation was given March 25, 2022 at Rosalind Franklin University for the Educational Series sponsored by the Office of...
11 views0 comments
shelleyamaves
Jun 11, 20201 min read
Medical Device Development and Commercialization
Medical devices product development has taken an added significance with COVID-19 as new technology is being investigated to provide new...
5 views0 comments
shelleyamaves
May 20, 20201 min read
How USP Panel and Expert Committee members help create better standards: A personal perspective
BioPhia principle consultant, Edward Chess shares his perspective on working with the USP on Expert Committees and Expert Panels. In...
1 view0 comments
shelleyamaves
Jun 3, 20190 min read
2 views0 comments