Life SciencesLiability

TL;DR

In a financing, acquisition, or IPO, the insurance program is read by people whose job is to find problems: investors, buyers' counsel, and underwriters. The recurring findings are D&O structure and run-off, claims-made lines with no tail plan, gaps in occurrence history, entities that are not named insureds, and contract insurance requirements that do not survive assignment. A specialist reads the program the way the other side will, before they do.

Financings · M&A · IPO

The insurance schedule goes in the data room. Someone on the other side will read every form.

Insurance rarely kills a deal. It does reprice them, delay them, and shift liabilities into escrows and special indemnities when a buyer finds a tail problem, a D&O structure that will not hold through a change in control, or a products history with a gap in it.

This page goes deeper than our IPO checklist and the multi-site CDMO acquisition answer. It covers what each side of the table should verify, and when.

Diligence finding 01 · D&O through a change in control

The D&O policy changes character the day the deal closes.

On a change in control, most D&O forms go into run-off for pre-closing wrongful acts. The target's directors need that run-off secured, usually for multiple years, and the merger agreement typically says so. Side A capacity matters most here, because it protects individuals when the company that used to indemnify them no longer exists in the same form. At an IPO the issue runs the other way: private D&O is replaced by a public program that must address registration statement exposure from the pricing date.

The review maps the current Side A/B/C structure, the change-in-control and run-off provisions, and what the transaction documents require, so the D&O terms are agreed before signing rather than discovered at closing.

Diligence finding 02 · Claims-made tail and occurrence history

Claims-made coverage stops answering for the past when the policy stops.

Life-sciences products, professional, and clinical lines are often written on a claims-made basis. When the seller's program ends at closing, claims arising from pre-closing products, services, or trials need either an extended reporting period or a buyer program that preserves the original retroactive date. Buyers also look for occurrence-form periods and gaps in history, because a missing year is an uninsured year.

The review builds a coverage timeline by line, identifies every claims-made trigger and retro date, and lays out the tail options and their tradeoffs for each side.

Diligence finding 03 · R&W insurance is not operating insurance

A rep and warranty policy covers the deal, not the business.

Representations and warranties insurance shifts loss from breached seller representations to an insurer, often replacing part of the traditional indemnity escrow. It typically excludes known issues, covenants, and areas the underwriter carves out after its own diligence, which can include specific product, regulatory, or pending-claim matters. The R&W underwriter will review the target's insurance program, and weaknesses there can become exclusions on the R&W policy.

The review prepares the operating program for that read and identifies where R&W exclusions are likely to leave the buyer relying on the target's own coverage or a special indemnity.

Diligence finding 04 · Entities and contracts after closing

Post-close, the named insureds and the contract certificates both have to be rebuilt.

Acquired entities need to be named on the buyer's program, or the target's program has to continue. Newly acquired organization clauses offer temporary automatic coverage, but usually with time limits, size thresholds, and exclusions for certain operations, and life-sciences targets often fall outside them. Foreign subsidiaries and IP-holding entities are easy to miss.

Customer, sponsor, and supply agreements frequently restrict assignment or require consent on a change in control, and their insurance clauses name a specific counterparty. The review lists each contract whose insurance requirements, additional insured status, or certificates must be reissued, so obligations do not lapse in the transition.

Carrier access

Transaction-ready programs are placed through specialty life-sciences markets.

D&O run-off, products tail, and post-close program integration all depend on markets that understand life-sciences exposure and transaction timelines. Specialty life-sciences markets can underwrite run-off, extended reporting, and integration on a deal schedule when the submission is complete and the exposures are explained clearly.

The review works for either side of the table. Sell-side, it prepares a clean schedule and closes findings before the data room opens. Buy-side, it reads the target as an underwriter would and quantifies what has to be fixed at or after closing.

Programs anchored in Texas with broader placement across the major US life-sciences clusters - including the New Jersey pharma corridor and the North Carolina (RTP) cluster.

Frequently asked

Common questions about insurance due diligence

What do investors and buyers ask for in insurance diligence?

Typically a schedule of all current policies with limits, retentions, forms, and policy periods; copies of the policies and endorsements; currently valued loss runs; a list of open and threatened claims and notices of circumstance; and the insurance requirements in material contracts. Buyers' counsel will also ask how claims-made coverage will respond after closing and whether any policy contains change-in-control or anti-assignment language.

What happens to D&O coverage on a change in control?

Most private and public company D&O forms convert to run-off on a change in control: the policy continues to respond to claims for wrongful acts before the transaction, but not after. The parties usually negotiate a multi-year run-off or tail for the target's directors and officers, often prepaid at closing and frequently required by the merger agreement. Side A coverage for individual directors deserves specific attention because it is the protection that survives when the company cannot indemnify.

What is the difference between D&O Side A, B and C?

Side A pays individual directors and officers when the company cannot or will not indemnify them. Side B reimburses the company when it does indemnify them. Side C covers the entity itself, broadly for private companies and typically limited to securities claims for public companies. In a transaction, the questions are how the limits are shared across the three, whether there is dedicated Side A capacity, and how the structure changes at an IPO.

Do we need tail coverage on products and E&O when we sell?

If those lines are written on a claims-made basis, yes, unless the buyer agrees to keep the retroactive date intact under its own program. Claims-made coverage responds to claims made while the policy is in force, so a product sold before closing that injures someone after closing may have no cover without an extended reporting period or continuity of the retro date. Occurrence-form products coverage does not carry this problem for the periods it covered.

Does R&W insurance replace the target's own insurance?

No. Representations and warranties insurance covers loss from breaches of the seller's representations in the purchase agreement. It generally excludes matters the deal team knew about, forward-looking covenants, and areas the underwriter specifically carves out, and it does not respond to ordinary operating claims. The target's products, professional, D&O, and property programs still have to be adequate in their own right.

When should diligence on our own program start?

Before the data room opens. Sell-side companies and companies preparing for a financing or IPO benefit from reading their own program as a buyer would, closing the findings, and preparing a clean schedule in advance. Findings discovered by the other side tend to become negotiation points.

Why operators choose this practice

  • Life sciences only

    Every placement passes through specialty life-sciences underwriters - not a general manufacturer or healthcare desk.

  • All 50 US states

    Programs placed nationally with deep practice content for the 16 states anchoring the major US life-sciences clusters.

  • End-of-day SLA

    Coverage review requests come back the same business day. MSA reads are typically half an hour or less.

  • Decoder + glossary

    Free MSA Decoder, 49-clause glossary, 60+ Q&A library. Designed for CFOs, GCs, and Quality leaders.

Complimentary diligence review

Read your program the way the other side will, before they do.

Send the schedule of insurance, policies, loss runs, and the deal context: financing, buy-side, sell-side, or IPO. A specialist returns a written read of the findings a buyer, investor, or underwriter is likely to raise.

Request the review

A specialist will reach out by end of business day.

Programs placed through A-rated specialty markets. Your specialist handles unlimited certificates of insurance, annual coverage reviews, and claims advocacy.