How we engage
We contract to the outcome you need. Choose the model that fits the work. We will tell you plainly if another one fits better.
A defined scope with deliverables, acceptance criteria and a fixed price or capped budget. Peritus directs the work and carries delivery risk.
When to use it. When the outcome can be specified up front, such as a qualification package, a readiness programme or a validation campaign.
A team of engineers assembled, mobilised and governed by Peritus, working as an extension of your engineering, quality and validation functions.
When to use it. When a programme needs several disciplines held together under one commercial relationship.
Senior engineers placed into your programme under Peritus technical oversight, with a clear path to move into managed delivery.
When to use it. When you need proven capacity quickly and want the option to scale into a managed team.
Senior practitioners engaged for design reviews, gap assessments, inspection readiness and decisions that need experienced technical judgement.
When to use it. When the question is what to do rather than who will do it.
Process
The same five stages apply whether we deliver a single protocol or a full facility programme.
We agree the objectives, deliverables, acceptance criteria and risks with your project lead. We also confirm the commercial model.
We assemble the team, complete site inductions and set up governance, reporting and document control.
We execute against the plan with milestone tracking, a live risk register and weekly reporting to your project lead.
We review every deliverable against your quality system and the agreed acceptance criteria before it is submitted.
We hand over documentation, knowledge and trained people so your site runs the system without us.
Why Peritus Consulting Partners
Our technical director has spent more than 20 years inside sterile manufacturing and has built, started and validated facilities himself.
We work to Therapeutic Goods Administration, United States Food and Drug Administration, European Medicines Agency and World Health Organization requirements.
Each engagement has a milestone plan, a live risk register and weekly reporting to your project lead.
We work on site, to your schedule, your quality system and your site procedures.
Tell us the scope, the site and the timing. A director will reply within one business day.