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Pharmaceutical and Vaccine Injury Litigation.

From adverse-event reporting through MDL coordination and, where it applies, a Vaccine Injury Compensation Program proceeding, the public story stays grounded in the clinical and regulatory record, not the manufacturer’s press release.

The Record

29 years, plaintiff-side only, including mass tort and MDL matters.

Direct Access

I answer every call and text myself.

The Defense Check

Free. The adverse-event record and regulatory filings, in writing, the same day, before you decide anything.

THE APPROACH

Adverse-event disclosures, recall and label-change history, MDL coordination and, where a claim proceeds through it, the Vaccine Injury Compensation Program, built on the clinical and regulatory filings.

What I Do

Communications around the adverse-event record, prior label changes and regulatory filings, from first filing through MDL coordination or a compensation-program hearing.

What You Get

Coverage sourced to the clinical and regulatory record, so it rests on the manufacturer’s own filings.

Why It Matters

The manufacturer’s safety statement is written to close the story. Yours should be what keeps the record straight.

See How This Applies to Your Case.

Text your case name and the defendant. Same day, you know what the defense is running. Free.

Text Karen — 415.359.4454 or call or email Karen

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