By clicking “Accept”, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts. View our Privacy Policy for more information.
AcceptDenyPreferences
Privacy

Insights & Industry News

Looking to for the latest insights and news in the healthcare industry? Our experts have you covered.
Check our articles on regulatory, clinical, and quality management for Biotech & MedTech.
Showing
0
Results
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
Clear results
No Results.
Try a different keyword.

Insights

NEXT Oncology joins Proxima Clinical Research Early Phase Oncology Network to Advance Investigational Cancer Therapies
Learn More

Insights

CMS Proposes TCET Pathway for Faster Medicare Access to Medical Innovations
Learn More

Insights

Outsourcing vs. Self-Management: Clinical Trial Management in Med Device & Drug Development
Learn More

Insights

FDA Issues Final Guidance: Device Software Functions and Premarket Submissions
Learn More

Insights

2023 And Me | The Proxima Post
Learn More

Insights

Addressing Bias in AI for Medical Applications: A Comprehensive Guide
Learn More

Insights

Galen Data Webinar: Reducing AI Risk to Secure Regulatory Approval
Learn More

Insights

The Proxima Playbook: Who Wants to be a Wellness Device?
Learn More

Insights

Why, When and How to Implement a Quality Management System (QMS)
Learn More

Insights

A Patient-Centric Approach to Overcoming Patient Recruitment Challenges in Oncology
Learn More

Insights

5 Key Strategies for Clinical Trial Patient Recruitment
Learn More

Insights

Expert Tips For Writing Your Clinical Trial Protocol
Learn More

Insights

510(k) or PMA: Should Your Medical Device Receive FDA Clearance or FDA Approval?
Learn More

Insights

Biotech and MedTech Funding Series: Funding an Oncology Startup with CPRIT
Learn More

Insights

Navigating the Pre-Market Approval Application Process for Your Class III Medical Device
Learn More

Insights

Greenlight Guru Webinar: Clinical Considerations for Software and Artificial Intelligence (AI) / Machine Learning (ML)
Learn More

Insights

M1 MedTech Accelerator Program Announces First Cohort of Early-Stage Medical Device Companies
Learn More

Insights

How AI (Artificial Intelligence) Dentistry is Transforming the Dental Device Industry
Learn More

Insights

M1 MedTech Accelerator Program Opens Applications to Early-Stage Medical Device Companies
Learn More

Insights

The Top 3 Things You Need To Know About Cardiovascular Devices Under The FDA
Learn More

Insights

Greenlight Guru Webinar: Is Regulation Necessary for Quality?
Learn More

Insights

Demystifying De Novo
Learn More

Insights

All About About ASCA
Learn More

Insights

What's So Special About The Special 510(k) Program?
Learn More

Insights

Project MedTech: The Overlap of Regulatory Strategy And Business Strategy with Isabella Schmitt
Learn More

Insights

The Conception of Ideas | Inventing Tomorrow Podcast
Learn More

Insights

The 510(k) Program – All About This Submission Type
Learn More

Insights

Kevin Coker: Top Five Considerations When Selecting a Contract Research Organisation
Learn More

Insights

Isabella Schmitt: The Time is Now for Pediatric Device Development to be Centerstage
Learn More

Insights

Major Guidance Changes to Artificial Intelligence and Machine Learning
Learn More

Insights

Greenlight Guru Webinar: Company Essentials: The Benefits of a Well-Developed Regulatory Plan
Learn More

Insights

Demystifying The Breakthrough Device Designation (BDD) & Safer Technologies (STeP) Processes with Greenlight Guru
Learn More

Insights

Top 3 Benefits of Breakthrough Device Designation or STeP Designation
Learn More

Insights

Global Medical Device Podcast: Comparing FDA's Breakthrough Devices Program & Safer Technologies Program
Learn More

Insights

Tackling ISO 10993-12 Biocompatibility
Learn More

Insights

Breakthrough Device Designation Reimbursement
Learn More

Insights

Design Controls Digest: 5 Phases of Design Controls You Need to Know
Learn More

Insights

Global Medical Device Podcast: Understanding and Handling Different Types of Feedback
Learn More

Insights

The Proxima Playbook: Understanding Your Biocompatibility Testing Requirements
Learn More

Insights

Global Medical Device Podcast: Why SaMD Companies Should be Leveraging Pre-Submissions to FDA
Learn More

Insights

Q2 Results Are In: Here are the Top Life Science Accelerators
Learn More

Insights

2020 MTI LIVE Webinar 5: Clinical Trials & Studies - Pre-Approval to Post-Market
Learn More

Insights

Global Medical Device Podcast: Addressing Clinical Trial Challenges & Concerns During Covid-19
Learn More

Insights

Global Medical Device Podcast: How to Integrate Usability into your Medical Device
Learn More

Insights

Global Medical Device Podcast: What You Need to Know About Clinical Evaluation & Validation for Software as a Medical Device (SaMD)
Learn More

Insights

"The Strategic Role of the Regulatory Professional", Regulatory Focus
Learn More

Insights

Global Medical Device Podcast: How to Establish a Solid Foundation for Fundraising and Product Success by Focusing on Regulatory
Learn More

Insights

Global Medical Device Podcast: 5 Tips for Hiring Medical Device Advisors
Learn More

Insights

FDA Rollouts Innovation and Improvements to Medical Device Sterilization
Learn More

Insights

Meet the Innovator: John Zellmer, MBA.
Learn More

Insights

Global Medical Device Podcast: Preparing for EU MDR
Learn More

Insights

Clinical Decision Support Software Guidance
Learn More

Insights

Safer Technologies Program (STeP) Breakdown
Learn More

Insights

Clinical Trials: Risky Business
Learn More

Insights

2019 MTI LIVE Webinar 5: Gathering Evidence: Clinical Trial Development & Design
Learn More

Insights

Why Your CRO Should Be With You From Concept to Commercialization
Learn More

Insights

Steps You Can Take to Answer If Your Product is A Drug or Medical Device
Learn More
Proxima Newsletter
Rants, raves and observations.
Occasionally an opinion or fact.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
Expertise
MedTech
Biotech
Resources
Resource Hub
Insights
Video Hub
Company
About
People
Careers
Company Updates
Privacy Policy
Connect
2450 Holcombe Blvd.
Houston, TX 77021
Hello@ProximaCRO.com
+1.281.306.3127
Proxima Clinical Research, Inc. (aka Proxima CRO) is a registered Delaware C Corp, headquartered in Houston, TX
© Copyright 2025 Proxima Clinical Research, Inc. All Rights Reserved.