About PendragonPharmaTech

Science first, then technology.

We are a specialist pharmaceutical technology and consulting company. Our work sits where laboratory science, regulation and digital delivery meet.

Our story

From the laboratory to pharmaceutical technology

PendragonPharmaTech was founded by a PhD medicinal chemist who moved from the laboratory into pharmaceutical IT, and has spent more than 20 years delivering technology for leading global pharmaceutical and life-sciences companies.

That work spans drug discovery and development, analytical laboratories, manufacturing, and clinical and real-world data: rolling out chromatography data systems and electronic lab notebooks, writing the requirements behind validated platforms, selecting laboratory vendors and leading multi-country digital programmes.

Along the way we kept seeing the same problem — reviewers spending hours re-checking records that were fine, while the few that mattered were hard to find. PxR is our answer to it.

20+ years in pharma & biotechPhD, Medicinal ChemistryCertified SAFe® 5 PO/PMCPAP (IIBA)GxP, CSV & 21 CFR Part 11UK, Switzerland & Europe
How we work

Four principles behind every engagement

Understand the science first

We start from the laboratory and the data, not from the tool. Requirements make sense when the people writing them understand the experiment.

Regulation by design

GxP, data integrity and validation are built in from the first requirement, so delivery stays inspection-ready instead of being fixed at the end.

Evidence over opinion

Decisions should be explainable and traceable. That applies to our recommendations and to PxR's rules alike.

Practical delivery

Agile, SAFe, waterfall or a hybrid — whichever fits your organisation, with outcomes your teams can actually adopt.

What we bring

Experience across the laboratory and digital landscape

Laboratory & scientific technology

  • Chromatography data systems
  • Electronic lab notebooks and LIMS
  • Spectroscopy and laboratory data workflows

GxP, validation & requirements

  • Computer system validation (IQ/OQ/PQ)
  • 21 CFR Part 11 and data integrity
  • User, business and functional requirements

Digital & process transformation

  • Process mapping and capability models
  • Real-world and patient data programmes
  • Vendor evaluation and selection

Delivery leadership & our own technology

  • Programme and product ownership
  • Multi-country, multi-vendor delivery
  • PxR, our review-by-exception platform

Working on something similar?

Tell us about your programme, validation challenge or data-review problem.