A Comprehensive Guide to MHRA Medical Device Registration (Steps, Budgeting, and Cost) | Operon Strategist Source Cluster: Operon Strategist Source Node: 3013502Time Stamp: Nov 27, 2023
Navigating Access to USFDA 510(k) Database: Step by Step Guide | Operon Strategist Source Cluster: Operon Strategist Source Node: 2975428Time Stamp: Nov 24, 2023
FDA’s Credibility Modelling Guidance for Medical Devices | Operon Strategist Source Cluster: Operon Strategist Source Node: 2975430Time Stamp: Nov 24, 2023
Indian Medical Technology Market Growth: Projected Surge to Rs 2,177.9 Billion by 2026 | Operon Strategist Source Cluster: Operon Strategist Source Node: 3013505Time Stamp: Nov 23, 2023
Guide to Getting a CDSCO Import License for Japanese Exporters of Medical Device | Operon Strategist Source Cluster: Operon Strategist Source Node: 3017792Time Stamp: Nov 20, 2023
Navigate US FDA Renewal Successfully: Establishment Registration Renewal | Operon Strategist Source Cluster: Operon Strategist Source Node: 2969929Time Stamp: Nov 10, 2023
Driving Innovation in Medical Devices Sector of India: What It Requires | Operon Strategist Source Cluster: Operon Strategist Source Node: 2969931Time Stamp: Nov 8, 2023
5 Essential Tips for Medical Device Manufacturing Site Selection (All You Need to Know) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2963778Time Stamp: Oct 30, 2023
India’s New IVD Device Classification Enhances Patient Safety and Regulation | Operon Strategist Source Cluster: Operon Strategist Source Node: 2959620Time Stamp: Oct 27, 2023
DoP’s Guidelines for Medical Devices Sector: Building a Skilled Workforce | Operon Strategist Source Cluster: Operon Strategist Source Node: 2956727Time Stamp: Oct 25, 2023
Comprehensive Guide to Stent Manufacturing (Step-by-Step Process) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2953807Time Stamp: Oct 23, 2023
SaMD Classification and Submission per US FDA: Expert Guide | Operon Strategist Source Cluster: Operon Strategist Source Node: 2946471Time Stamp: Oct 20, 2023
Information of Medical Devices Assembly in India (Know About Regulatory Compliances) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2941295Time Stamp: Oct 16, 2023
CE Marking for Software as Medical Device (SaMD) – Operon Strategist Source Cluster: Operon Strategist Source Node: 2932850Time Stamp: Oct 13, 2023
6 Month Extension for CDSCO Class C & D Medical Device License | Operon Strategist Source Cluster: Operon Strategist Source Node: 2931073Time Stamp: Oct 12, 2023
A Quick Guide to the Medical Device Regulatory Requirements in Lebanon (Compliance and Success) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2927671Time Stamp: Oct 9, 2023
CE Mark Vs FDA Approval For Medical Devices | Which Is Better? | Operon Strategist Source Cluster: Operon Strategist Source Node: 2919732Time Stamp: Oct 6, 2023
Healthcare Transformation: FDA’s Move to Regulate LDTs (Laboratory Developed Tests) as Medical Devices | Operon Strategist Source Cluster: Operon Strategist Source Node: 2917135Time Stamp: Oct 4, 2023
Wearable Medical Device Registration in Singapore (Step-by-Step Guidance) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2899825Time Stamp: Sep 25, 2023
FDA Published Draft Guidance on Best Practices for Selecting Predicate Devices for 510(k) Notifications Source Cluster: Operon Strategist Source Node: 2896531Time Stamp: Sep 23, 2023