Caitlin | VP Marketing at FissionTop 5 Common Pitfalls in FDA Pre-Submission Meetings and How to Avoid Them — FissionIntroduction to FDA Pre-Submission MeetingsAug 7
Webfrog IT Services TeaminI3CGLOBAL BlogsUS FDA Registration and Approval For Coffee by I3CGLOBALIn the ever-evolving landscape of food regulations, coffee businesses must adhere to specific guidelines set by the U.S. Food and Drug…Feb 11
Darek DawdaHow Power Trip became its own power trip: A report on the state of the MDMA Therapy orchardIn the beginning, all was well. Yes, there were hiccups, minor problems, and even one major ethics violation during the early…Aug 6Aug 6
MedcryptinMedcrypt Medical Device Cybersecurity BlogsFDA is issuing deficiency letters- why you should care (Part 1/4)By Naomi Schwartz, Medcrypt VP of ServicesMar 12Mar 12
Webfrog IT Services TeaminI3CGLOBAL BlogsFDA Approval for Skin Care Products by I3CGlobalAt present, the healthcare industry in Saudi Arabia is quickly developing. While the global demand for reliable medical supplies grows…Jul 30Jul 30
Caitlin | VP Marketing at FissionTop 5 Common Pitfalls in FDA Pre-Submission Meetings and How to Avoid Them — FissionIntroduction to FDA Pre-Submission MeetingsAug 7
Webfrog IT Services TeaminI3CGLOBAL BlogsUS FDA Registration and Approval For Coffee by I3CGLOBALIn the ever-evolving landscape of food regulations, coffee businesses must adhere to specific guidelines set by the U.S. Food and Drug…Feb 11
Darek DawdaHow Power Trip became its own power trip: A report on the state of the MDMA Therapy orchardIn the beginning, all was well. Yes, there were hiccups, minor problems, and even one major ethics violation during the early…Aug 6
MedcryptinMedcrypt Medical Device Cybersecurity BlogsFDA is issuing deficiency letters- why you should care (Part 1/4)By Naomi Schwartz, Medcrypt VP of ServicesMar 12
Webfrog IT Services TeaminI3CGLOBAL BlogsFDA Approval for Skin Care Products by I3CGlobalAt present, the healthcare industry in Saudi Arabia is quickly developing. While the global demand for reliable medical supplies grows…Jul 30
Duncan RossFDA revises observations for Kimera Labs’ XoGlo® product due to IND approvalOn March 7th 2024, Kimera Labs received a communication from the FDA stating that due to our May 2023 Investigational New Drug approval we…Mar 20
Pavan AnnéinZS AssociatesThe evolution of CDx: Navigating regulatory pathways, co-development strategies and future…Multiple avenues currently exist to expedite the regulatory approval process, read more about navigating regulatory pathways and…Jul 9
Evalytics LabsFDA Clears Rejoyn: A New Era for App-Based Depression TreatmentThe U.S. Food and Drug Administration (FDA) recently made a groundbreaking move by green-lighting Rejoyn, the first prescription therapy…Apr 7