| name | regulatory-affairs-head |
| description | Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Use when developing regulatory strategy, preparing FDA 510(k)/PMA/De Novo submissions, planning EU MDR CE marking, coordinating global market access, or monitoring regulatory intelligence. Provides pathway analysis, submission management, timeline planning, and cross-functional regulatory leadership.
|
| license | MIT + Commons Clause |
| metadata | {"version":"1.0.0","author":"borghei","category":"compliance","domain":"regulatory-strategy","updated":"2026-03-31T00:00:00.000Z","tags":["regulatory-affairs","fda","eu-mdr","market-access","regulatory-strategy"]} |
Head of Regulatory Affairs
Regulatory strategy development, submission management, and global market access for medical device organizations.
Regulatory Strategy Workflow
The agent develops regulatory strategy aligned with business objectives and product characteristics.
Workflow: New Product Regulatory Strategy
- Gather product information -- collect intended use, device classification (risk level), technology platform, target markets, and timeline from stakeholders.
- Identify applicable regulations per target market:
- FDA (US): 21 CFR Part 820, 510(k)/PMA/De Novo
- EU: MDR 2017/745, Notified Body requirements
- Other markets: Health Canada, PMDA, NMPA, TGA
- Determine optimal regulatory pathway using the pathway selection matrix below -- compare submission types, assess predicate device availability, evaluate clinical evidence requirements.
- Develop regulatory timeline with milestones and critical path dependencies.
- Estimate resource requirements -- budget, personnel (FTEs), external consultants/CRO.
- Identify regulatory risks and define mitigation strategies for each.
- Obtain stakeholder alignment -- present strategy for executive approval.
- Validation checkpoint: Strategy document approved; timeline accepted by all stakeholders; resources allocated and confirmed.
Regulatory Pathway Selection Matrix
| Factor | 510(k) | De Novo | PMA |
|---|
| Predicate Available | Yes | No | N/A |
| Risk Level | Low-Moderate | Low-Moderate | High |
| Clinical Data | Usually not required | May be required | Required |
| Review Time | 90 days (MDUFA) | 150 days | 180 days |
| User Fee | ~$22K (2024) | ~$135K | ~$440K |
| Best For | Me-too devices | Novel low-risk | High-risk, novel |
Example: Regulatory Strategy Output
REGULATORY STRATEGY
Product: CardioSense Wearable ECG Monitor
Version: 1.0
Date: 2026-03-12
1. PRODUCT OVERVIEW
- Intended use: Continuous ECG monitoring for arrhythmia detection
- Device classification: Class II (FDA), Class IIa (EU MDR)
- Technology: Single-lead ECG with ML-based AF detection
2. TARGET MARKETS
| Market | Priority | Timeline |
|--------|----------|-------------|
| USA | 1 | Q3 2026 |
| EU | 2 | Q1 2027 |
| Canada | 3 | Q2 2027 |
3. REGULATORY PATHWAY
- FDA: 510(k) — Predicate: AliveCor KardiaMobile (K142743)
- EU: Class IIa via Annex IX (QMS) + Annex XI Part A (Product)
- Rationale: Established predicate supports SE argument;
MDR IIa classification per Rule 10 (active diagnostic)
4. CLINICAL EVIDENCE STRATEGY
- Requirements: SE comparison + analytical performance data
- Approach: Literature review for AF detection + bench study
5. RISKS AND MITIGATION
| Risk | Probability | Impact | Mitigation |
|--------------------------|-------------|--------|-------------------------------|
| FDA requests clinical | Medium | High | Pre-Sub meeting to align |
| NB capacity delay | High | Medium | Engage NB by Q4 2025 |
| ML algorithm as SaMD | Medium | High | Follow FDA AI/ML SaMD guidance|
FDA Submission Workflow
The agent prepares and submits FDA regulatory applications following established pathways.
Workflow: 510(k) Submission
- Confirm 510(k) pathway suitability -- verify predicate device identified, substantial equivalence supportable, no new intended use or technology concerns.
- Schedule Pre-Submission (Q-Sub) meeting if novel technology, uncertain predicate, or complex testing is involved.
- Compile submission package:
- Cover letter and administrative information
- Device description and intended use
- Substantial equivalence comparison
- Performance testing data
- Biocompatibility (if patient contact, per ISO 10993)
- Software documentation (if applicable, per IEC 62304)
- Labeling and IFU
- Conduct internal review -- quality check all sections against FDA checklist.
- Prepare eCopy per current FDA format requirements.
- Submit via FDA ESG portal with user fee payment.
- Monitor MDUFA clock and respond to AI/RTA requests within deadline.
- Validation checkpoint: Submission accepted (RTA complete); MDUFA goal date received; tracking system updated.
Workflow: PMA Submission
- Confirm PMA pathway -- Class III device or no suitable predicate; clinical data strategy defined.
- Complete IDE clinical study if required -- IDE approval, protocol execution, study report.
- Conduct Pre-Submission meeting with FDA.
- Compile PMA submission -- administrative/device information, manufacturing information, nonclinical studies, clinical studies, labeling.
- Submit original PMA application.
- Address FDA questions and deficiency letters within specified timeframes.
- Prepare for FDA facility inspection -- coordinate with Quality team.
- Validation checkpoint: PMA approved; approval letter received; post-approval requirements documented.
FDA Submission Timeline
| Milestone | 510(k) | De Novo | PMA |
|---|
| Pre-Sub Meeting | Day -90 | Day -90 | Day -120 |
| Submission | Day 0 | Day 0 | Day 0 |
| RTA Review | Day 15 | Day 15 | Day 45 |
| Substantive Review | Days 15-90 | Days 15-150 | Days 45-180 |
| Decision | Day 90 | Day 150 | Day 180 |
Common FDA Deficiencies
| Category | Common Issues | Prevention |
|---|
| Substantial Equivalence | Weak predicate comparison | Strong SE argument upfront |
| Performance Testing | Incomplete test protocols | Follow recognized standards |
| Biocompatibility | Missing endpoints | ISO 10993 risk assessment |
| Software | Inadequate documentation | IEC 62304 compliance |
| Labeling | Inconsistent claims | Early labeling review |
See: references/fda-submission-guide.md
EU MDR Submission Workflow
The agent achieves CE marking under EU MDR 2017/745.
Workflow: MDR Technical Documentation
- Confirm device classification per MDR Annex VIII rules.
- Select conformity assessment route based on class:
- Class I: Self-declaration
- Class IIa/IIb: Notified Body involvement
- Class III: Full NB assessment
- Select and engage Notified Body (for Class IIa+) -- evaluate scope, capacity, experience, and timeline.
- Compile Technical Documentation per Annex II:
- Device description and specifications
- Design and manufacturing information
- GSPR checklist (General Safety and Performance Requirements)
- Benefit-risk analysis and risk management (ISO 14971)
- Clinical evaluation per Annex XIV
- Post-market surveillance plan
- Establish and document QMS per ISO 13485.
- Submit application to Notified Body.
- Address NB questions and coordinate audit logistics.
- Validation checkpoint: CE certificate issued; Declaration of Conformity signed; EUDAMED registration complete.
Clinical Evidence Requirements by Class
| Class | Clinical Requirement | Documentation |
|---|
| I | Clinical evaluation (CE) | CE report |
| IIa | CE with literature focus | CE report + PMCF plan |
| IIb | CE with clinical data | CE report + PMCF + clinical study (some) |
| III | CE with clinical investigation | CE report + PMCF + clinical investigation |
Notified Body Selection Criteria
| Criterion | Consideration |
|---|
| Scope | Device category expertise |
| Capacity | Availability and review timeline |
| Experience | Track record in your technology |
| Geography | Proximity for audits |
| Cost | Fee structure transparency |
| Communication | Responsiveness and clarity |
See: references/eu-mdr-submission-guide.md
Global Market Access Workflow
The agent coordinates regulatory approvals across international markets.
Workflow: Multi-Market Submission Strategy
- Define target markets based on business priorities and revenue projections.
- Sequence markets for efficient evidence leverage:
- Phase 1: FDA + EU (reference markets)
- Phase 2: Recognition markets (Canada via MDSAP, Australia via TGA)
- Phase 3: Major markets (Japan PMDA, China NMPA)
- Phase 4: Emerging markets
- Identify local requirements per market -- clinical data acceptability, local agent/representative needs, language and labeling requirements.
- Develop master technical file with localization plan.
- Establish in-country regulatory support.
- Execute parallel or sequential submissions per sequencing strategy.
- Track approvals and coordinate product launches.
- Validation checkpoint: All target market approvals obtained; registration database updated; launch dates confirmed.
Market Priority Matrix
| Market | Size | Complexity | Recognition | Priority |
|---|
| USA | Large | High | N/A | 1 |
| EU | Large | High | N/A | 1-2 |
| Canada | Medium | Medium | MDSAP | 2 |
| Australia | Medium | Low | EU accepted | 2 |
| Japan | Large | High | Local clinical | 3 |
| China | Large | Very High | Local testing | 3 |
| Brazil | Medium | High | GMP inspection | 3-4 |
See: references/global-regulatory-pathways.md
Regulatory Intelligence Workflow
The agent monitors and responds to regulatory changes affecting the product portfolio.
Workflow: Regulatory Change Management
- Monitor regulatory sources -- FDA Federal Register, EU Official Journal, MDCG guidance, Notified Body communications, industry associations (AdvaMed, MedTech Europe).
- Assess relevance to current product portfolio and pipeline.
- Evaluate impact -- timeline to compliance, resource requirements, product changes needed.
- Develop compliance action plan with owners and deadlines.
- Communicate to affected stakeholders across functions.
- Implement required changes within established timelines.
- Document compliance status for management review and audit readiness.
- Validation checkpoint: Compliance action plan approved; changes implemented on schedule; no gaps at next audit.
Regulatory Monitoring Sources
| Source | Type | Frequency |
|---|
| FDA Federal Register | Regulations, guidance | Daily |
| FDA Device Database | 510(k), PMA, recalls | Weekly |
| EU Official Journal | MDR/IVDR updates | Weekly |
| MDCG Guidance | EU implementation | As published |
| ISO/IEC | Standards updates | Quarterly |
| Notified Body | Audit findings, trends | Per interaction |
Decision Frameworks
Pathway Selection Decision Tree
Is predicate device available?
|
Yes-+-No
| |
v v
Is device Is risk level
substantially Low-Moderate?
equivalent? |
| Yes-+-No
Yes-+-No | |
| | v v
v v De Novo PMA
510(k) Consider required
De Novo
or PMA
Pre-Submission Meeting Decision
| Factor | Schedule Pre-Sub | Skip Pre-Sub |
|---|
| Novel Technology | Yes | |
| New Intended Use | Yes | |
| Complex Testing | Yes | |
| Uncertain Predicate | Yes | |
| Clinical Data Needed | Yes | |
| Well-established | | Yes |
| Clear Predicate | | Yes |
| Standard Testing | | Yes |
Regulatory Escalation Criteria
| Situation | Escalation Level | Action |
|---|
| Submission rejection | VP Regulatory | Root cause analysis, strategy revision |
| Major deficiency | Director | Cross-functional response team |
| Timeline at risk | Management | Resource reallocation review |
| Regulatory change | VP Regulatory | Portfolio impact assessment |
| Safety signal | Executive | Immediate containment and reporting |
Tools and References
Scripts
| Tool | Purpose | Usage |
|---|
| regulatory_tracker.py | Track submission status and timelines | python regulatory_tracker.py --help |
python scripts/regulatory_tracker.py --status active --format markdown
python scripts/regulatory_tracker.py --overdue --notify
References
| Document | Content |
|---|
| fda-submission-guide.md | FDA pathways, requirements, review process |
| eu-mdr-submission-guide.md | MDR classification, technical documentation, clinical evidence |
| global-regulatory-pathways.md | Canada, Japan, China, Australia, Brazil requirements |
| iso-regulatory-requirements.md | ISO 13485, 14971, 10993, IEC 62304, 62366 requirements |
Key Performance Indicators
| KPI | Target | Calculation |
|---|
| First-time approval rate | >85% | (Approved without major deficiency / Total submitted) x 100 |
| On-time submission | >90% | (Submitted by target date / Total submissions) x 100 |
| Review cycle compliance | >95% | (Responses within deadline / Total requests) x 100 |
| Regulatory hold time | <20% | (Days on hold / Total review days) x 100 |
Related Skills
Troubleshooting
| Problem | Likely Cause | Resolution |
|---|
| Regulatory tracker shows "No existing data file found" | Data file does not exist at the expected path | Create an initial submissions JSON file or use the tracker to add a first submission. The tool creates the file on first save. |
| Submission status shows as PLANNING when it should be SUBMITTED | Status not updated after submission | Update the submission record with submission_status: SUBMITTED and submission_date. The tracker does not auto-detect FDA ESG submission status. |
| Overdue notification fires for approved submission | actual_approval_date field not populated | Update the record with the actual approval date. The tracker compares target_approval_date against today when actual_approval_date is null. |
| 510(k) pathway selected but clinical data still needed | Novel technology or uncertain predicate | Schedule a Pre-Submission (Q-Sub) meeting with FDA. Novel technologies or complex testing may require clinical evidence even under the 510(k) pathway. |
| Notified Body timeline exceeds plan | NB capacity constraints (common in 2025-2026) | Engage the NB as early as possible (6+ months before target submission). The number of designated MDR NBs has grown to ~50 as of 2024, but capacity remains tight for complex device classes. |
| EUDAMED registration blocked | EUDAMED modules not yet mandatory or data upload issues | Develop a secure process for uploading device data into EUDAMED. Certain modules become mandatory in 2026. Prepare data structures proactively. |
| Multi-market submission timeline keeps slipping | Sequential submissions creating cascading delays | Where possible, shift to parallel submission strategy. Use FDA + EU as reference markets and leverage MDSAP for recognition markets (Canada, Australia, Japan, Brazil). |
Success Criteria
- First-time regulatory approval rate exceeds 85% across all submission types (510(k), PMA, De Novo, CE marking)
- Regulatory submission timelines met for 90%+ of submissions (submitted by target date)
- Pre-Submission meetings scheduled and completed for all novel technology, uncertain predicate, or complex testing submissions
- FDA review cycle compliance exceeds 95% (responses to AI/RTA/deficiency requests submitted within deadline)
- EU MDR Technical Documentation complete and accepted by Notified Body with no critical findings on first review
- Global market access strategy documented with phased market sequencing, resource estimates, and risk mitigation for each target jurisdiction
- Regulatory intelligence monitoring active for all applicable jurisdictions with change assessments completed within 30 days of publication
Scope & Limitations
In Scope:
- Regulatory strategy development for medical devices across FDA, EU MDR, and global markets
- FDA submission management (510(k), PMA, De Novo, Q-Sub/Pre-Submission)
- EU MDR conformity assessment route selection and Notified Body engagement
- Global market access planning and multi-market submission sequencing
- Regulatory intelligence monitoring and change management
- Submission timeline planning and milestone tracking
- Regulatory pathway selection decision frameworks
Out of Scope:
- Clinical trial design, execution, or data analysis (the skill addresses clinical evidence strategy but not clinical operations)
- Detailed technical file content creation (use mdr-745-specialist for GSPR checklists, Annex II documentation)
- Quality system management (use quality-manager-qms-iso13485 for QMS processes)
- Post-market surveillance program execution (the skill defines PMS strategy but execution is managed by PMS teams)
- Reimbursement strategy or health technology assessment (HTA) submissions
- Patent or intellectual property strategy related to regulatory pathways
- In vitro diagnostic (IVD) specific regulatory requirements under IVDR 2017/746
Integration Points
| Skill | Integration |
|---|
| mdr-745-specialist | Detailed EU MDR technical requirements, GSPR checklists, Annex VIII classification rules, and EUDAMED registration |
| fda-consultant-specialist | FDA submission deep expertise including QMSR alignment, HIPAA, cybersecurity guidance, and 510(k)/PMA specifics |
| quality-manager-qms-iso13485 | QMS certification is a prerequisite for MDR conformity assessment and supports FDA QMSR compliance |
| risk-management-specialist | ISO 14971 risk management file is required for both FDA submissions and EU MDR Technical Documentation |
| quality-manager-qmr | Regulatory changes affecting the QMS are management review inputs; QMR coordinates compliance across jurisdictions |
Tool Reference
regulatory_tracker.py
Tracks regulatory submission status, timelines, and overdue notifications across all markets.
| Flag | Required | Description |
|---|
--status | No | Filter submissions by status: active, planning, submitted, approved, all |
--overdue | No | Show only submissions past their target approval date without an actual approval date |
--notify | No | Generate notification alerts for overdue or at-risk submissions |
--format | No | Output format: markdown for formatted text, omit for default display |
Note: The tracker operates on a regulatory_submissions.json data file (default path). Submissions are added and updated programmatically through the RegulatoryTracker class API. The tool supports submission types: FDA_510K, FDA_PMA, FDA_DE_NOVO, EU_MDR_CE, ISO_CERTIFICATION, GLOBAL_REGULATORY.
