Medical Device & IVD Blog
Indonesia Medical Device Registration Cost: LAR Pricing Models and Cash Flow
Compare Indonesia LAR pricing models for medical device registration, including hourly, annual, and flat-fee structures, AKD/AKL cash flow, and importation fee mechanics.
ISO 27001 for Medical Device Companies: Information Security Implementation Guide
Learn how medical device companies can implement ISO 27001, align ISMS controls with ISO 13485 and FDA cybersecurity expectations, and plan certification.
ISO/TR 24971 for Medical Devices: Practical Guidance for Applying ISO 14971
Practical guide to ISO/TR 24971:2020 for applying ISO 14971, including hazard identification, risk analysis methods, benefit-risk decisions, and cybersecurity.
EU MDR Literature Search Protocol for Clinical Evaluation and CER Evidence
Build an EU MDR literature search protocol for clinical evaluation, covering Article 61, Annex XIV, MEDDEV methodology, PICO, databases, appraisal, PRISMA, and Notified Body expectations.
Malaysia Medical Device Registration Cost 2026: MAR Pricing and 3-Year Budget
Buyer-side guide to Malaysia medical device registration costs, comparing MAR hourly, annual, and flat-fee pricing models with 3-year cash flow scenarios and CAB-MDA-MAR fee structure.
Medical Device Distribution Agreements: Regulatory Clause Guide
Draft distribution agreements with EU MDR importer duties, FDA distributor controls, territory and exclusivity terms, PMS, vigilance, quality, and negotiation clauses.
Medicare NCD vs LCD for Medical Devices: Coverage Strategy Guide
Compare Medicare NCD and LCD pathways for medical devices, including evidence requirements, timelines, RAPID, Coverage with Evidence Development, MACs, and coverage strategy.
Mexico Medical Device Registration Cost: MRH Pricing Guide (2026)
Compare Mexico MRH pricing models for medical device registration, including flat fees, hourly billing, three-year cash flow scenarios, switching steps, RFP points, and COFEPRIS pathways.
New Zealand Medsafe Medical Device Registration and WAND Guide
Register medical devices in New Zealand through Medsafe WAND, including sponsor duties, GHTF classification, adverse event reporting, labeling, TTMRA reliance, timelines, and costs.
NTAP Application Guide for Medical Devices: Criteria, Timeline, and Strategy
Guide to CMS NTAP for medical devices, covering newness, cost, clinical improvement criteria, MEARIS submission, timelines, payment calculation, and pathway strategy.
Pakistan DRAP Medical Device Registration: Classification and Import Licensing
Register medical devices in Pakistan with DRAP classification, establishment licensing, local agent duties, Urdu labeling, fees, timelines, and PMS.
Patient-Reported Outcomes in Device Trials: PRO Validation and FDA/EU Expectations
Use PRO instruments in medical device trials with fit-for-purpose validation, endpoint planning, FDA CDRH expectations, EU MDR evidence, and submission strategy.
Risk Management File vs Risk Management Report: ISO 14971 Documentation Explained
Clear guide to ISO 14971 risk management files and reports, including required contents, traceability expectations, document structure, and audit findings.
SaMD vs SiMD vs Embedded Software: Classification, Documentation, and Regulatory Strategy
Guide to classifying SaMD, SiMD, and embedded medical device software, with IMDRF definitions, IEC 62304 risk classes, FDA and EU MDR pathways, and documentation strategy.
Sample Size Calculation for Medical Device Clinical Investigations: Methods and Examples
Practical guide to sample size justification for device clinical investigations, covering ISO 14155, EU MDR Annex XV, FDA IDE expectations, common study designs, and worked examples.
Singapore Medical Device Registration Cost 2026: Registrant Pricing Guide
Compare Singapore Registrant pricing models for HSA medical device registration, including hourly, annual, and flat-fee options with 3-year cash flow examples.
State of the Art Review for Medical Devices: SOTA and CER Comparator Guide
Build a defensible SOTA review for EU MDR clinical evaluation, with comparator selection, benchmark devices, outcome parameters, MDCG evidence hierarchy, and CER examples.
Statistical Analysis Plan for Medical Device Trials: SAP Endpoints and Estimands
Develop a medical device SAP covering endpoints, estimands, analysis populations, missing data, sensitivity analyses, multiplicity, timing, and FDA/EU MDR expectations.
Sunshine Act Open Payments Reporting for MedTech Companies: Compliance Guide
Guide to Sunshine Act and Open Payments compliance for device manufacturers, including covered recipients, reportable payments, 2026 thresholds, CMS submissions, penalties, and audits.
Switzerland Device Registration Cost 2026: CH-REP Fees and Pricing Models
Compare Swiss CH-REP pricing models for 2026, including Pure Global flat fees, hourly billing, registration-plus-annual fees, and 3-year cash flow scenarios.