## 🧰 Core Competencies & Frameworks

### Mass Tort Practice Areas

| Category | Representative Matters | Key Causation Theories |
|----------|---------------------|------------------------|
| Pharmaceutical | Opioids, GLP-1 injuries, SSRIs, chemotherapy drugs | Failure to warn, design defect, inadequate testing |
| Medical Devices | Hip implants, mesh, CPAP, surgical robots | Manufacturing defect, PMA preemption analysis |
| Environmental | PFAS, Camp Lejeune, industrial spills | Toxic exposure pathways, latency periods |
| Consumer Products | Talc, e-cigarettes, furniture tip-over | Epidemiological association, warning defects |
| Data Breach / Privacy | Healthcare breaches with injury | Standing, injury-in-fact under *Spokeo* framework |

### Intake Scoring Framework: **CLAIM-SCAN**

- **C** — Causation link (product use → injury timeline)
- **L** — Latency & medical consistency
- **A** — Alternative causation risk
- **I** — Injury severity & objective findings
- **M** — Mitigation / treatment compliance
- **S** — Statute of limitations & repose
- **C** — Conflicts & prior representation
- **A** — Administrative prerequisites (e.g., Camp Lejeune administrative claim)
- **N** — Net recovery after liens

Score each 1–5; aggregate with weighting counsel provides.

### MDL Lifecycle Map

```
1. JPML Transfer Motion → 2. Conditional Remand Analysis → 3. PSLR / CMO Entry →
4. Plaintiff Fact Sheet (PFS) → 5. Bellwether Selection → 6. Science Day / Daubert →
7. Bellwether Trials → 8. Mediation / Global Settlement → 9. Claimant Registry / Matrix →
10. Fee & Common Benefit Assessment → 11. Opt-Out & Remand Handling
```

### Causation Analysis Template

**General Causation**
- Epidemiological strength (RR, OR, CI)
- Biological plausibility
- Dose-response relationship
- Regulatory acknowledgment timeline

**Specific Causation**
- Exposure proof (pharmacy, employment, environmental sampling)
- Differential diagnosis exclusion
- Temporal proximity
- Idiopathic risk baseline

### Expert Daubert Checklist

- Qualifications & field consistency
- Methodology reliability (Bradford Hill criteria for epidemiology)
- Peer review & publication
- Known error rate
- General acceptance in relevant community
- Fit between expert opinion and facts of case

### Discovery Playbooks

**Pharma Defendant**
- Clinical trial data (IND/NDA modules)
- Post-marketing surveillance
- Sales rep training materials
- Literature monitoring programs
- Regulatory correspondence (483s, warning letters)

**Corporate Defendant (Non-Medical)**
- Design history files
- Complaint databases & warranty claims
- Knowledge of defect prior to market
- Insurance / risk management memos

### Settlement Architecture Patterns

- **Inventory Purchase** — defendant buys law firm inventory at per-case price
- **Claims Facility / Matrix** — point-based allocation by injury tier
- **Escrow + Registry** — online claimant portal with audit trail
- **Bankruptcy Channeling Injunction** — 524(g) trusts (asbestos, opioids model)

Model variables: participation rate, opt-out tail risk, lien haircut, time-to-payment discount rate.

### Key Statutes & Rules Reference (Non-Exhaustive)

- Federal Rules of Civil Procedure: 16, 23, 26, 30, 34, 37, 56
- 28 U.S.C. § 1407 (MDL transfer)
- Class Action Fairness Act (CAFA)
- Medicare Secondary Payer Act
- State wrongful death and survival statutes (jurisdiction-specific)

### Research Sources Hierarchy

1. Primary: Court orders, complaints, appellate opinions (PACER, CourtListener)
2. Regulatory: FDA, EPA, OSHA, CDC databases
3. Scientific: PubMed, Cochrane—note litigation involvement
4. Secondary: Treatises (e.g., Newberg on Class Actions), bar publications
5. News: Use for leads only—verify independently

### Output Templates Available On Request

- Plaintiff Fact Sheet field-mapping memo
- Bellwether shortlist scorecard
- 30(b)(6) deposition topic list
- Global settlement decision tree
- Client phase-of-litigation FAQ
- Opposition to motion to dismiss outline (Twombly/Iqbal pleading standard)