Regulatory Affairs Head

Head of Regulatory Affairs

Regulatory strategy development, submission management, and global market access for medical device organizations.

Table of Contents

• Regulatory Strategy Workflow
• FDA Submission Workflow
• EU MDR Submission Workflow
• Global Market Access Workflow
• Regulatory Intelligence Workflow
• Decision Frameworks
• Tools and References

Regulatory Strategy Workflow

Develop regulatory strategy aligned with business objectives and product characteristics.

Workflow: New Product Regulatory Strategy

1. Gather product information:
   • Intended use and indications
   • Device classification (risk level)
   • Technology platform
   • Target markets and timeline
2. 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
3. Determine optimal regulatory pathway:
   • Compare submission types (510(k) vs De Novo vs PMA)
   • Assess predicate device availability
   • Evaluate clinical evidence requirements
4. Develop regulatory timeline with milestones
5. Estimate resource requirements and budget
6. Identify regulatory risks and mitigation strategies
7. Obtain stakeholder alignment and approval
8. Validation: Strategy document approved; timeline accepted; resources allocated

Regulatory Pathway Selection Matrix

Regulatory Strategy Document Template

REGULATORY STRATEGY

Product: [Name]   Version: [X.X]   Date: [Date]

1. PRODUCT OVERVIEW
   Intended use: [One-sentence statement of intended patient population, body site, and clinical purpose]
   Device classification: [Class I / II / III]
   Technology: [Brief description, e.g., "AI-powered wound-imaging software, SaMD"]

2. TARGET MARKETS & TIMELINE
   | Market | Pathway        | Priority | Target Date |
   |--------|----------------|----------|-------------|
   | USA    | 510(k) / PMA   | 1        | Q1 20XX     |
   | EU     | Class [X] MDR  | 2        | Q2 20XX     |

3. REGULATORY PATHWAY RATIONALE
   FDA: [510(k) / De Novo / PMA] — Predicate: [K-number or "none"]
   EU:  Class [X] via [Annex IX / X / XI] — NB: [Name or TBD]
   Rationale: [2–3 sentences on key factors driving pathway choice]

4. CLINICAL EVIDENCE STRATEGY
   Requirements: [Summarize what each market needs, e.g., "510(k): bench + usability; EU Class IIb: PMCF study"]
   Approach: [Literature review / Prospective study / Combination]

5. RISKS AND MITIGATION
   | Risk                         | Prob | Impact | Mitigation                        |
   |------------------------------|------|--------|-----------------------------------|
   | Predicate delisted by FDA    | Low  | High   | Identify secondary predicate now  |
   | NB audit backlog             | Med  | Med    | Engage NB 6 months before target  |

6. RESOURCE REQUIREMENTS
   Budget: $[Amount]   Personnel: [FTEs]   External: [Consultants / CRO]

FDA Submission Workflow

Prepare and submit FDA regulatory applications.

Workflow: 510(k) Submission

1. Confirm 510(k) pathway suitability:
   • Predicate device identified (note K-number, e.g., K213456)
   • Substantial equivalence (SE) argument supportable on intended use and technological characteristics
   • No new intended use or technology concerns triggering De Novo
2. Schedule and conduct Pre-Submission (Q-Sub) meeting if needed (see Pre-Sub Decision)
3. Compile submission package checklist:
   • Cover letter with device name, product code, and predicate K-number
   • Section 1: Administrative information (applicant, contact, 510(k) type)
   • Section 2: Device description — include photos, dimensions, materials list
   • Section 3: Intended use and indications for use
   • Section 4: Substantial equivalence comparison table (see example below)
   • Section 5: Performance testing — protocols, standards cited, pass/fail results
   • Section 6: Biocompatibility summary (ISO 10993-1 risk assessment, if patient contact)
   • Section 7: Software documentation (IEC 62304 level, cybersecurity per FDA guidance, if applicable)
   • Section 8: Labeling — final draft IFU, device label
   • Section 9: Summary and conclusion
4. Conduct internal review and quality check against FDA RTA checklist
5. Prepare eCopy per FDA format requirements (PDF bookmarked, eCopy cover page)
6. Submit via FDA ESG portal with user fee payment
7. Monitor MDUFA clock and respond to AI/RTA requests within deadlines
8. Validation: Submission accepted; MDUFA date received; tracking system updated

Substantial Equivalence Comparison Example

Workflow: PMA Submission

1. Confirm PMA pathway:
   • Class III device or no suitable predicate
   • Clinical data strategy defined
2. Complete IDE clinical study if required:
   • IDE approval
   • Clinical protocol execution
   • Study report completion
3. Conduct Pre-Submission meeting
4. Compile PMA submission checklist:
   • Volume I: Administrative, device description, manufacturing
   • Volume II: Nonclinical studies (bench, animal, biocompatibility)
   • Volume III: Clinical studies (IDE protocol, data, statistical analysis)
   • Volume IV: Labeling
   • Volume V: Manufacturing information, sterilization
5. Submit original PMA application
6. Address FDA questions and deficiencies
7. Prepare for FDA facility inspection
8. Validation: PMA approved; approval letter received; post-approval requirements documented

FDA Submission Timeline

Common FDA Deficiencies and Prevention

See: references/fda-submission-guide.md

EU MDR Submission Workflow

Achieve CE marking under EU MDR 2017/745.

Workflow: MDR Technical Documentation

1. Confirm device classification per MDR Annex VIII
2. Select conformity assessment route based on class:
   • Class I: Self-declaration
   • Class IIa/IIb: Notified Body involvement
   • Class III: Full NB assessment
3. Select and engage Notified Body (for Class IIa+) — see selection criteria below
4. Compile Technical Documentation per Annex II checklist:
   • Annex II §1: Device description, intended purpose, UDI
   • Annex II §2: Design and manufacturing information (drawings, BoM, process flows)
   • Annex II §3: GSPR checklist — each requirement mapped to evidence (standard, test report, or justification)
   • Annex II §4: Benefit-risk analysis and risk management file (ISO 14971)
   • Annex II §5: Product verification and validation (test reports)
   • Annex II §6: Post-market surveillance plan
   • Annex XIV: Clinical evaluation report (CER) — literature, clinical data, equivalence justification
5. Establish and document QMS per ISO 13485
6. Submit application to Notified Body
7. Address NB questions and coordinate audit
8. Validation: CE certificate issued; Declaration of Conformity signed; EUDAMED registration complete

GSPR Checklist Row Example