Looking for Technically Write IT (TWi)? We rebranded to Altuent.

Built for the demands of pharma and life sciences

With 15+ years of experience supporting global life sciences companies, our teams understand GxP environments, regulatory expectations, and the documentation standards that quality and regulatory leaders demand.

  • We have ISO9001 and IS27001 accreditation.
  • We work within the guidelines of GMP, ICH and ISO standards
  • Ensure quality and compliance with SLAs and KPIs
  • Deep domain expertise in pharma
  • Experienced with MSAT, Quality and Product Lifecycle teams
  • Scalable teams that ramp quickly without compromising quality

“Altuent played a pivotal role in supporting our digital transformation in technical content production and management.


Their expertise in content operations and governance was invaluable.”

Head of Technical Content | Global Pharma Enterprise

Experienced in manufacturing‑led CPV

We work alongside MSAT, manufacturing, and technical teams who feed into quality and APRs, focusing on the parts of CPV that often slow organisations down.

Rapid Ramp-Up

We fall in line with your next drug cycle — not the one after. Our team of life science process engineers hit the ground running.

Minimal SME Burden

Your subject matter experts are stretched thin. Our process engineers and writers free up your SME time by being proactive throughout the lifecycle. We already know what to ask, and when to prevent rewrites and time delays.

Identifying content workflow efficiencies

We don’t just write reports, we automate manual data tasks that your team hasn’t had time to address, reducing errors and accelerating every cycle.

Built for real‑world CPV pressure

CPV is a regulatory requirement, but in practice it’s often delayed by SME workload, fragmented data, and review bottlenecks. We step in to keep CPV moving in real time.

Data You Can Trust

Our experts verify and validate every data point. Whether it’s manually entered, pulled from Excel, or exported from CSV files, before it reaches your CPV report.

Meet the experts driving your CPV report transformation

Jennifer Bailey

Senior Information Developer

Jennifer Bailey

Senior Information Developer

M.Sc. graduate with over 15 years project management and technical writing experience in pharmaceutical and medical diagnostic GMP environments, grant management and the renewable energy sector.
Main areas of expertise include technical writing, workflow management, process improvement, root cause analysis, impact assessment, change control, risk assessment and training.

Amukelani Baloyi

Process Engineer

Eibhlin Hegarty

Team Lead

Sarah O’Brien

Medical Communications Specialist

Cassidy Ryan

AI Solutions Consultant

Cassidy Ryan

AI Solutions Consultant

Cassidy is an AI solutions consultant with a technical background. She has worked with DITA and content management systems, and more recently has focused on AI ready content. Cassidy is from Oregon but now lives in Tipperary. She enjoys reading science fiction, singing, and crochet.

Sean Power

AI Knowledge Consultant