Pharmaceutical & Life Sciences practice

Validated systems for regulated science.

Life sciences technology carries a validation burden most sectors never face. We deliver GxP-aligned systems with computer system validation, 21 CFR Part 11 controls, electronic batch records and serialisation — documented to withstand inspection.

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Less time locating documents

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Less manual document handling

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Audit-traceable records

Sector challenges

What pharmaceutical & life sciences clients bring us

Left column is the problem as it is usually described to us. Right column is what we actually build in response.

Challenge

Validation documentation produced manually for every change

Our response

Risk-based CSV approach with automated test evidence capture and traceability matrices generated from the pipeline.

Challenge

Batch records on paper, slowing release and inviting error

Our response

Electronic batch records with in-process checks, deviation capture and review-by-exception release.

Challenge

Serialisation and track-and-trace obligations across markets

Our response

Serialisation platform with aggregation, market-specific reporting and partner data exchange.

Challenge

Research and trial data fragmented across systems and sites

Our response

Governed research data platform with lineage, controlled access and reproducible analysis environments.

Compliance

Frameworks we design against

Regulatory obligations common in pharmaceutical & life sciences. We treat these as architectural inputs from the first design session.

  • 21 CFR Part 11
  • GxP (GMP / GCP / GLP)
  • EU Annex 11
  • GAMP 5
  • DSCSA & EU FMD serialisation
  • HIPAA

Pharmaceutical & Life Sciences enquiry

Let us talk about your pharmaceutical & life sciences programme

You will speak with someone who has delivered in this sector before — not a generalist reading a capability deck.

Book a discovery call Email the team

Princeton, NJ · Tiruchirappalli, India · +1 (609) 681-2414