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Vyom Infotec Solutions

Vyom Infotec Pharma LIMS Solutions

Sample Pooling Workflows

Pharma labs can reduce redundant testing and enhance accuracy with smart pooling workflows in LIMS.

Capabilities:

  • Custom pooling logic & rule-based config
  • Automated workflows with tracking & audit
  • Auto retests for failed pools
  • Instrument integration for result mapping
  • Full validation of pooled processes

Client Benefits:

  • Lower costs, faster TAT
  • Fewer analyst errors
  • GMP/GxP compliant
  • Barcoded traceability

Use Cases:

  • Water/environment monitoring
  • Bulk raw material testing
  • Vaccine sample screening

Stability Study Modules

Automated ICH-compliant stability modules for traceable, error-free study management in LIMS.

Capabilities:

  • ICH zone & pull schedule config
  • Test order auto-generation
  • Chamber linking & monitoring
  • Trending & exception reporting
  • Training for QA & users

Client Benefits:

  • Zero missed timepoints
  • Audit-ready documentation
  • Centralized visibility
  • Global ICH alignment

Use Cases:

  • API & finished product stability
  • Photostability testing

Automated COA Generation

Speed up batch release with digital COA generation and integrated approval workflows.

Capabilities:

  • Product-specific COA templates
  • Auto population of test results
  • ERP system integration
  • E-signature approvals
  • Localization support

Client Benefits:

  • Fast, error-free COAs
  • System-validated QA checks
  • Consistent global formats

Use Cases:

  • Raw/in-process/final product COAs
  • Export-ready documents

Instrument Integration with LIMS

Validated Empower & lab equipment integration to eliminate manual data risks.

Capabilities:

  • Empower-to-LIMS interfaces
  • Balance/pH/Spectro mapping
  • Result automation & exception flags
  • Integration qualification support

Client Benefits:

  • No manual data entry
  • Faster reviews
  • Live equipment tracking

Use Cases:

  • Chromatography (assay/purity)
  • Dissolution automation

Environmental Monitoring Modules

End-to-end EM setup to comply with cleanroom and aseptic processing guidelines.

Capabilities:

  • Location/route setup (ISO rooms)
  • Support for viable & non-viable tests
  • Deviation workflows & alerts
  • Trending, heatmaps, ID linkage

Client Benefits:

  • Automated cleanroom tracking
  • Contamination trend alerts
  • Paperless, audit-ready EM

Use Cases:

  • Sterile manufacturing (vaccines)
  • QC lab cleanroom control