Pharma & Life Sciences
Material records, batch activities and quality documents need to describe the same product. Haloglide connects these operational records so teams can review the evidence behind a batch without rebuilding its history from disconnected files.
Book a demoFor the people doing the work
Each team contributes the evidence that belongs to its part of the work. The next team can follow the record without starting again.
Material or sample lot
Sample and material teams
Identify the material or sample lot, its source and recorded quantity. Attach relevant documents and location context so the next team can find the evidence for the material in front of them.
Assessment context
Laboratory and operations
Record configured readings and activities against the relevant lot. Attach laboratory results and supporting documents, retaining the context needed for your quality team to interpret them.
Batch evidence review
Quality and assurance
Follow incoming records, recorded activities and evidence for the batch under review. Use selected evidence for partner questions while keeping formal release decisions in the organisation’s approved process.
The connected journey
Source lot and documents
Processing and recorded readings
Results with their lot context
Quality and partner assessment
Which inputs contributed to the batch?
Create and connect material lots through Production Manager. Keep quantities, units and input to output relationships available through processing. This provides operational lineage; any use within a regulated process requires assessment against your validation and quality requirements.
Can the reviewer understand what happened?
Flight Recorder brings receiving, processing, inspection, storage and dispatch events into the lot history. Keep supporting documents with the activity or product they explain, rather than relying on a separate folder to supply context.
Can the next team find the right record?
Use Halo ID to connect a marked unit or lot to its operational record. Halo Connect supports selected published views and read only lot handovers. Required pharmaceutical exchange formats and integrations must be assessed for the intended use; the product identity alone does not establish regulatory compliance.
Where does the evidence end and the decision begin?
Haloglide supports connected evidence for review. It does not replace validated quality systems, authorised batch release, clinical judgment or legally required medicine verification networks. Define the intended use, access requirements and validation obligations with your quality team before deployment.
Each role needs a different view of the connected record. These illustrative examples show what belongs in each review.
Illustrative evidence
Review the recorded relationships and activities.
Shared on your terms
Illustrative workflows and records use demonstration data. Photography illustrates industry activities, not customer operations.
Put the platform to work
Start with the records your team already needs. Keep them connected for the next buyer question, partner handover or assurance review.
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