Pharma & Life Sciences.
Traceability from batch to shelf.
Drema builds software for pharmaceutical and life sciences operations: batch and serialisation traceability, quality management, distributor and field-force tooling, and research data capture. Validation and traceability shape everything here — a system that cannot evidence what happened is a liability, not an asset.
What this sector
actually deals with.
Quality events are tracked in spreadsheets. Batch traceability requires three people and a day of searching. Field representatives report on paper. When an audit or a recall happens, assembling the evidence becomes the emergency rather than the event itself.
Systems this sector
keeps needing.
The parts of a pharma & life sciences platform that carry the weight. Not everything at once — we build the one that unblocks you first.
Batch and serialisation tracking
Full genealogy from raw material through to distributed pack.
Quality management
Deviations, CAPA, change control and audit findings with enforced workflow.
Distributor and stockist portals
Ordering, inventory visibility and returns across the channel.
Field force tooling
Offline-capable apps for representatives calling on clinicians and chemists.
Research data capture
Structured, validated entry with a complete change history.
Where the work
pays for itself.
The problems pharma & life sciences teams bring us most often. If one of these is costing you money today, it is worth a conversation.
Recall readiness
Identifying every affected pack and its location in minutes rather than days.
Audit preparation
Evidence assembled continuously rather than reconstructed before an inspection.
Channel visibility
Knowing real stock positions downstream instead of inferring from despatch.
Trial data collection
Validated capture with audit trails suitable for regulatory review.
Not on this list? Sector problems rarely fit a template — tell us yours.
What shapes a build
in this sector.
These are the things a generalist team discovers late and prices badly. We design around them from the first week.
- Good practice guidelines and computer system validation expectations
- 21 CFR Part 11 style controls for electronic records and signatures
- Serialisation and track-and-trace requirements for exports
- Change control with documented testing evidence
How we usually
engage here.
The services pharma & life sciences clients most often start with.
Pharma & Life Sciences
questions.
Straight answers, including where we are not the right team.
Can you deliver validated systems?
We build to validation requirements and produce the documentation, testing evidence and traceability matrices your quality team needs. The validation itself is signed off by your quality function, not by us, and we structure delivery so that is straightforward.
How do you handle electronic signatures?
Signature events are bound to an authenticated identity, timestamped and immutable, with the meaning of the signature recorded. Audit trails cannot be edited or deleted by any user role, including administrators.
Can this work offline for field staff?
Yes, and it must. Field representatives frequently work without connectivity, so we build local persistence with conflict-aware sync rather than assuming a live connection.
Do you work with existing ERP and LIMS?
Yes. Most engagements integrate with SAP or similar plus laboratory systems, and we build an integration layer so their constraints do not propagate through the new software.
Building for pharma & life sciences?
Bring the problem as it actually is, constraints included.
You will get a straight answer on whether we are the right team.