India Revolutionizes Drug & Medical Device Approval Process: Streamlined Path to Innovation | Operon Strategist Source Cluster: Operon Strategist Source Node: 2549915Time Stamp: Apr 18, 2024
CDSCO Important Update: Mandatory Registration of Class C and D Medical Devices (Transition to Licensing) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2547576Time Stamp: Apr 15, 2024
Guide to Uzbekistan Medical Device Registration: Navigate the Regulatory Landscape with Expert Assistance | Operon Strategist Source Cluster: Operon Strategist Source Node: 2547578Time Stamp: Apr 15, 2024
Ensuring Safety and Efficacy: The Importance of Medical Device Software Validation and Verification | Operon Strategist Source Cluster: Operon Strategist Source Node: 2542984Time Stamp: Apr 12, 2024
Navigating the Regulatory Landscape of Drug Device Combination Products (Insights & Strategies) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2538787Time Stamp: Apr 8, 2024
Performance Evaluation for IVD Device: Step-by-Step Process | Operon Strategist Source Cluster: Operon Strategist Source Node: 2538789Time Stamp: Apr 5, 2024
Global Opportunities for Medical Device Manufacturers: India, LATAM, and African Markets | Operon Strategist Source Cluster: Operon Strategist Source Node: 2530010Time Stamp: Mar 29, 2024
FDA’s AI Integration Strategy for Revolutionizing Medical Products | Operon Strategist Source Cluster: Operon Strategist Source Node: 2526472Time Stamp: Mar 26, 2024
Ultimate Guide to Cleanroom Setup for Medical Device Industry (Expert Tips) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2525374Time Stamp: Mar 25, 2024
Mandatory Online Submission of PSURs for Medical Devices Implemented | Operon Strategist Source Cluster: Operon Strategist Source Node: 2522435Time Stamp: Mar 22, 2024
A Comprehensive Guide to Obtaining CDSCO Loan Licenses for Medical Devices | Operon Strategist Source Cluster: Operon Strategist Source Node: 2522437Time Stamp: Mar 22, 2024
CDSCO Online Safety Reporting: Mandatory Compliance for Medical Device Manufacturers | Operon Strategist Source Cluster: Operon Strategist Source Node: 2521198Time Stamp: Mar 21, 2024
Concerns Raised by Parliamentary Panel on Quality of Used Medical Devices | Operon Strategist Source Cluster: Operon Strategist Source Node: 2520216Time Stamp: Mar 20, 2024
Navigating European NB Opinion for Drug-Device Combination Products (A Comprehensive Guide) | Operon Strategist Source Cluster: Operon Strategist Source Node: 2520218Time Stamp: Mar 18, 2024
Haryana’s Medical Device Manufacturing Policy 2024 Aims for ₹3000 Crore Investment | Key Objectives & Components)Operon Strategist Source Cluster: Operon Strategist Source Node: 2520281Time Stamp: Mar 18, 2024
A Comprehensive Guide for the Risk Analysis of Drug-Device Combination Products | Operon Strategist Source Cluster: Operon Strategist Source Node: 2517371Time Stamp: Mar 15, 2024
Ujjain Medical Device Park: 5 Companies Invest ₹176 Crore | Operon Strategist Source Cluster: Operon Strategist Source Node: 2512451Time Stamp: Mar 12, 2024
5 Tips for Successful Medical Device Registration Across Global Markets | Operon Strategist Source Cluster: Operon Strategist Source Node: 2511073Time Stamp: Mar 11, 2024
Safe and Secure: HIPAA Compliance and Cybersecurity for Medical Software Devices | Operon Strategist Source Cluster: Operon Strategist Source Node: 2509598Time Stamp: Mar 9, 2024
Understanding Notified Body Criteria for EU MDR Technical Documentation | Operon Strategist Source Cluster: Operon Strategist Source Node: 2506141Time Stamp: Mar 4, 2024