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KPO & Knowledge Services

On-demand analytical capacity for life sciences teams.

Researchers, writers and domain specialists who take defined workstreams off your desk and return finished work, scaled to your workload rather than a fixed retainer.

The problem

Senior specialists spend a third of their week on work someone else could do.

A medical affairs lead formats references. A regulatory director chases a literature search. A market access manager rebuilds a competitor table that changes monthly. None of it is a poor use of the hour in isolation, and collectively it is the reason the strategic work slips.

The usual fix is a headcount request that takes two quarters and arrives after the peak has passed. The alternative most teams try, a generalist outsourcer, produces work that has to be checked so thoroughly the saving disappears.

We staff each workstream with people whose qualifications match the judgement it requires, and put a documented quality review in front of every deliverable.

Talk to a specialist

Tell us the problem. A specialist replies, not a form robot.

What we do

What we cover.

MW

Medical Writing

Regulatory, clinical and scientific writing to house or agency standard.

What that means for you

  • Writers with relevant scientific qualifications
  • Consistent with your templates and style
  • Reviewed before it reaches you
PUB

Publishing Support

Submission-ready formatting, publishing and lifecycle document management.

What that means for you

  • Format issues caught before the submission window
  • Version control that holds across a portfolio
  • Capacity available at the peak, not after it
DI

Drug Information

Structured drug information programmes and response handling.

What that means for you

  • Built by people who have stood these programmes up inside global organisations
  • Oversight that is technical rather than administrative
  • Documented and auditable responses
MI

Market Intelligence

Competitive and market analysis on a cadence you set.

What that means for you

  • Analysts who understand the therapeutic context
  • Updated on your schedule rather than a vendor calendar
  • Findings you can put in front of a leadership team

100%

Deliverables through documented quality review

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We do not publish quotes we have not been given permission to use.

Questions

Questions we get asked before the first call.

How do you keep quality consistent?

Every workstream that needs pharmacological or medical-science judgement is staffed with people whose qualifications match the task, and every deliverable passes a documented quality review before it reaches the client.

Can you work inside our templates and systems?

Yes, and it is usually the better arrangement. Working in your document management system keeps version control intact and avoids a reconciliation step at the end.

What is the minimum engagement?

Smaller than most people expect. A single deliverable is a reasonable way to test us, and we would rather earn a larger scope than negotiate one up front.

How do you handle confidential and pre-publication material?

Named teams, restricted access, and the same controls we apply on clinical engagements. Where a client requires it, work stays entirely within their environment.

Is this delivered onshore or offshore?

Usually a blend, with senior review onshore. For work that does not require US presence, offshore delivery is where the cost advantage is real rather than nominal.

Related

Where to go next.

Clinical & CRO

Where medical writing meets the study it reports on.

Read more ›

Regulatory

Authoring the documents behind a submission.

Read more ›

Services overview

All five pillars.

Read more ›

Send us one requisition.

Judge us on the shortlist, not the sales deck.

Request talent+1 (848) 371-9666