Vodori

Vodori Vodori's Pepper Cloud® streamlines how life science companies get critical content to key audiences including patients and healthcare providers.

It is one connected platform of content review, sales and MSL enablement, and analytics software. Pharmaceutical, biopharma, medical device, and diagnostic companies are under immense pressure to get content to market quickly, maintain compliance, and achieve maximum productivity. Pepper Cloud is a connected software platform that is easy to use and empowers life science companies around the world to:

- Review and approve content quickly
- Ensure process compliance
- Give sales reps, MSLs, and distributors easy, tailored access to approved content
- Optimize content and processes with actionable data
- Get ongoing support and consultation from a world-class customer service team

The Pepper Cloud Product Suite includes Pepper Flow® for promotional and medical information review and approval, Pepper Folio® for sales and MSL enablement, and Pepper Insights® for analytics and reporting. Our software is used by thousands of life science professionals in more than 50 countries worldwide who trust Vodori’s ongoing commitment to excellence in product usability and customer service. For more information, visit vodori.com.

What’s the one question you’d ask about promotional review in 2026?Is our review time normal for a company our size? Wha...
11/04/2026

What’s the one question you’d ask about promotional review in 2026?

Is our review time normal for a company our size? What’s a realistic first pass approval rate? Why do our feedback rounds take longer than our reviews?

On November 16, Jessy Horrell and Lauren Woods start the Q&A with questions submitted at registration.

Ask yours when you sign up and we’ll answer it live:
https://hubs.li/Q04Dhv-m0

The median MLR workflow in Vodori’s 2026 benchmarks report takes 12.6 days. The average takes 18.5. That gap is where th...
10/29/2026

The median MLR workflow in Vodori’s 2026 benchmarks report takes 12.6 days. The average takes 18.5. That gap is where the useful questions start.

A single number can’t tell you whether your team is fast, slow, or simply different from the organizations it’s being measured against.

On Monday, November 16, Jessy Horrell, VP of Professional Services, and Lauren Woods, Director of Customer Success, go past the headline numbers in the 2026 State of Promotional Review report, with Director of Marketing, Annalise Ludtke.

They’ll cover topics including:

- Where the time in a review cycle actually goes – Is it review? Revisions? Something else?
- How to compare your organization against the various cohorts in the report
- Rework and AI – With more companies using AI than ever before, why are typos still the most common reason for recirculation?
- How peers are balancing speed and accuracy as scrutiny rises

Monday, November 16, 11:00 AM to 12:00 PM EST. Register and get the full report: https://hubs.li/Q04CQ3sF0

Most teams assume a slow MLR review is a reviewer problem. The 2026 benchmark data says otherwise.Typos and errors drive...
10/27/2026

Most teams assume a slow MLR review is a reviewer problem. The 2026 benchmark data says otherwise.

Typos and errors drive 23.9% of the reasons content gets sent back. Branding issues add another 13.5%. Neither needs a reviewer to catch.

See where MLR rework comes from, and how much of it is preventable: https://hubs.li/Q04BcgQt0

The 2026 State of Promotional Review Benchmarks Report is live, and this year, the diamonds are in the details.The avera...
10/13/2026

The 2026 State of Promotional Review Benchmarks Report is live, and this year, the diamonds are in the details.

The average workflow takes 18.5 days from preparation to approval. Helpful guidance, but it doesn't describe the majority of life science companies. Content in France averages 35.1 days. Regional content across APAC averages 8.5.

New this year: data by subcohort, market reach, and region.

Explore the report: https://hubs.li/Q04zX8xZ0

Knowing how long your MLR review takes is a start. Knowing how often it took more than one round is the part most teams ...
10/07/2026

Knowing how long your MLR review takes is a start. Knowing how often it took more than one round is the part most teams are missing.

Review duration and first pass approval only make sense when read together. One tells you how long. The other tells you how often you had to do it twice.

First pass approval is new to this year's benchmarks report. The 2026 data lands October 13.

The claim nobody reviewed was on tab three.Not hidden. Just behind a tab no one clicked during review.A brochure shows y...
09/29/2026

The claim nobody reviewed was on tab three.

Not hidden. Just behind a tab no one clicked during review.

A brochure shows you everything at once. A web page doesn't. That's why web content needs its own checklist.

https://hubs.li/Q04wy5JR0

The same agency sends the same outdated logo every time. You catch it, fix it in five minutes, and move on.That five min...
09/23/2026

The same agency sends the same outdated logo every time. You catch it, fix it in five minutes, and move on.

That five minutes never gets logged anywhere. Neither does the next one.

It's why a review process can look fine on paper and still feel broken to everyone in it.

Read more: https://hubs.li/Q04wv1hC0

Thank you to everyone who joined us on Monday for The AI Efficiency Trap webinar.Jason Cober of Compliance Forward and A...
09/17/2026

Thank you to everyone who joined us on Monday for The AI Efficiency Trap webinar.

Jason Cober of Compliance Forward and Annalise Stromsta Ludtke, M.A.l of Vodori worked through the impacts of AI generated content on the MLR review process, and what organizations are doing about it.

Missed it? The full session is now on demand: https://hubs.li/Q04xHqdL0

Four days out.On Monday, Jason Cober of Compliance Forward and Annalise Ludtke of Vodori are working through what AI is ...
09/10/2026

Four days out.

On Monday, Jason Cober of Compliance Forward and Annalise Ludtke of Vodori are working through what AI is actually doing to the MLR process. The operational view rather than the optimistic one: where it genuinely helps, where it quietly moves work downstream, and what to have in place before scaling it.

Monday, September 14, 2:00 to 3:00 PM EST. Register here: https://hubs.li/Q04x1Fch0

Cannot make it live? Register anyway and we will send you the recording.

Your reviewers flagged the same missing reference three submissions in a row.Each correction was captured, time-stamped,...
09/08/2026

Your reviewers flagged the same missing reference three submissions in a row.

Each correction was captured, time-stamped, and fully auditable. But none of that knowledge helped prevent the issue from appearing again.

Your system of record contains years of regulatory decisions. Today, most of that institutional knowledge remains trapped in the record instead of informing the next piece of content.

The Regulated Content Intelligence Platform™ is designed to change that.

Learn more: https://hubs.li/Q04wv4G50

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60606

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Wednesday 8am - 5pm
Thursday 8am - 5pm
Friday 8am - 5pm

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