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Life Sciences · U.S. Mid-Atlantic

Biologics Manufacturing Suite Recovery

Two biologics production suites where validation was planned as one late block nobody could measure.

Owner
Confidential
Region
U.S. Mid-Atlantic
Market
Life Sciences
Our role
Schedule recovery and CQV planning
Size
2 production suites
Delivery
EPCM
Duration
30 months
Status
In progress · 2026
The challenge

What is at stake.

Construction was nearly complete, but commissioning, qualification and validation were shown as a single bar. The team could not tell whether the licensed production date was still possible.

Schedule30 monthsIn progress · finish 2026
202420252026
Today
Start
2024
Planned finish
2026
Time elapsed
96%
Our role

What we are doing.

Beck Franklin's role: schedule recovery and cqv planning. We advise and measure; the contractor builds.

01

CQV broken down

We broke commissioning, qualification and validation into measurable steps by system.

02

Protocol tracking

Every protocol is tracked from draft to approval to execution to report.

03

Recovery sequence

A recovery sequence runs the two suites in parallel where systems allow.

04

Weekly progress

Progress is reported weekly to the site leadership team.

Results

Where it stands.

2Suites with measurable CQV paths
340Protocols tracked
WeeklyProgress to site leadership
30Months to licensed production

You cannot recover what you cannot measure. Breaking validation into steps gave the team something to manage.

Life sciences scheduler, Beck Franklin
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Life Sciences

Facing something like this?

Send us the schedule and the date that matters. We will tell you what is driving it and where you can still act. Repeat or similar projects qualify for our discounted Program Rate.