Know which drug and device claims already have medical treatment on record
Ask prospective clients whether they can name the drug or device involved, when the complication occurred, and what treatment followed, then collect medical records and prescription or device documentation before you ever pick up the phone.
Preview your dangerous drugs and medical devices intake
Explore 7 questions from the Dangerous Drugs and Medical Devices template. This interactive preview uses illustrative scoring and sample attachments. Open the full survey to try the complete intake.
What a qualified dangerous drugs and medical devices lead should tell you
Claims involving harm allegedly caused by a prescription drug, over-the-counter medication, or an implanted or used medical device, qualified by confirming the drug or device involved, the injury or complication it caused, and the medical treatment that followed.
- Take Prescription Or Over-
- Believe That Drug Or
- Receive Medical Treatment, Diagnosis,
- Injury Or Complication Happen
- Identify Name Drug Or
- Have Out- -Pocket Costs,
- Represented By Lawyer This
The questions your team needs answered
Every dangerous drugs and medical devices intake asks these — and why each one matters.
| Question | Why it matters |
|---|---|
| Did you take a prescription or over-the-counter drug, or have a medical device implanted or used on you? | A 'yes' confirms the claim actually involves a drug or device exposure, which is the threshold fact this entire case type depends on. |
| Do you believe that drug or device caused you a serious injury, complication, or new medical condition? | This isolates prospective clients who believe the drug or device caused genuine harm rather than a minor side effect, which is the core of a viable claim. |
| Did you receive medical treatment, a diagnosis, surgery, hospitalization, or ongoing care because of that injury or complication? | Documented treatment, diagnosis, surgery, or hospitalization gives you the medical record you'll need to substantiate damages. |
| Did the injury or complication happen within the last 3 years? | A recent injury keeps the claim inside a viable filing window, while an older one signals a case that needs a faster legal review. |
| Can you identify the name of the drug or device (or the manufacturer/brand) you think is involved? | Naming the drug, device, or manufacturer lets you match the claim to known litigation or recalls before investing consultation time. |
| Did you have out-of-pocket costs, lost income, long-term symptoms, disability, or other significant impacts because of the injury? | Quantifiable financial, medical, or lifestyle impact signals a case with real damages worth pursuing. |
| Are you currently represented by a lawyer for this drug or device injury? | A prospective client already represented by counsel for this injury is a lower-fit lead you likely don't want to schedule a duplicate consultation for. |
How Cliont scores dangerous drugs and medical devices leads
Configured answer weights help your team prioritize follow-up. Your team reviews each submission and decides the next step.
Value signals
- Take Prescription Or Over-: yes
- Believe That Drug Or: yes
- Receive Medical Treatment, Diagnosis,: yes
- Injury Or Complication Happen: yes
- Identify Name Drug Or: yes
- Have Out- -Pocket Costs,: yes
Lower-fit signals
- Represented By Lawyer This: no
See an example lead handoff
Illustrative lead details and score show how a submission can reach your team.
Hip Implant Injury Lead
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They explain the matter
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You get a ready lead
Scored and qualified — waiting for you to win it.
Built for dangerous drugs and medical devices workflows
| Cliont capability | Dangerous Drugs And Medical Devices application |
|---|---|
| Weighted lead scoring | Combines answers on drug/device use, belief of serious injury, and documented medical treatment to push leads with substantiated harm toward High Priority. |
| Lower-fit flagging | Automatically tags prospective clients who say they're already represented by a lawyer for this injury, so staff can skip scheduling a duplicate consultation. |
| Document upload capture | Collects medical records, prescription or device packaging photos, and hospitalization documentation directly in the intake before the claim reaches your CRM. |
| Statute-of-limitations flagging | Uses the injury-timing question to surface claims outside the recent window for a faster attorney review rather than treating every claim the same. |
| CRM routing | Sends each scored claim, along with its score, band, and uploaded medical documentation, directly into your CRM instead of a generic inbox. |
Example dangerous drugs and medical devices lead scenarios
Illustrative situations explain the intake questions and possible follow-up.
Recent implant failure needing revision
Prospective client had a device implanted, needed revision surgery within the past year, and can name the manufacturer, so the intake pushes the score toward High Priority.
Old prescription injury outside the window
The complication happened more than three years ago, which the intake flags for a fast statute-of-limitations review instead of scoring it as high as a recent case.
Already retained by another lawyer
The prospective client answers yes to already having counsel for this drug or device injury, and the intake tags it as lower-fit so you can decline or deprioritize instead of booking a duplicate consultation.
Suspected drug reaction, brand unknown
The prospective client believes a medication caused a serious reaction but can't yet name the drug or manufacturer, so the intake flags it for follow-up rather than treating it as disqualifying.
Symptoms without a diagnosis yet
The prospective client suspects a device is causing problems but hasn't had it diagnosed, treated, or documented by a physician, which lowers the score until medical evidence exists.
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More personal injury intake templates
Dangerous Drugs and Medical Devices lead-intake FAQs
How does the intake handle prospective clients who already have a lawyer?
The catalog asks directly whether the prospective client is currently represented for this drug or device injury, and a 'yes' is weighted as a lower-fit signal so those leads still reach your CRM but flagged for deprioritization.
What happens if someone can't name the exact drug or device?
Not being able to identify the drug, device, or manufacturer lowers the score slightly but doesn't disqualify the lead, since the name can often be confirmed later from uploaded medical records or prescription documentation.
Does the intake account for statute of limitations concerns?
Yes, the intake asks whether the injury or complication happened within the last three years so older claims are flagged for a quicker legal look rather than scored the same as recent ones.
What documentation does the intake collect before a claim reaches my CRM?
Prospective clients are prompted to upload medical records, prescription or device packaging details, and any surgical or hospitalization paperwork tied to the injury.
Can the intake tell a minor side effect apart from a serious injury claim?
The intake asks whether the prospective client believes the drug or device caused a serious injury, complication, or new medical condition, and that answer carries significant weight in the score.
Does the intake capture financial or lifestyle impact, not just medical harm?
Yes, it asks about out-of-pocket costs, lost income, long-term symptoms, or disability tied to the injury, which factors into how the lead is scored.
Turn dangerous drugs and medical devices visitors into qualified cases
Give every dangerous drugs and medical devices visitor a guided intake instead of a dead contact form — and get a scored, qualified lead before you book a consultation.