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More Than Solutions

Comprehensive Digital Solutions For Your Business

From analytics to development, we provide end-to-end solutions tailored to your unique requirements.

Development

Microbiology & Lab Testing

Industrial Microbiological Testing

Contract microbiological testing for pharma, food, cosmetic and manufacturing operations — raw materials, in-process, water, environment and finished product against pharmacopoeial and ISO methods.

Raw Material Microbiological Testing

Incoming ingredient screening for total counts, yeasts and moulds and specified pathogens, with risk-based sampling plans, supplier qualification and skip-lot programmes.

Finished Product Microbiological Testing

Batch release testing against IP, USP, Ph. Eur., FSSAI and BIS specifications — microbial limits, specified organisms, sterility and statistical trend analysis.

Environmental Monitoring Microbiology

Cleanroom and facility EM programmes — viable air, settle plates, contact plates and personnel monitoring, with risk-based site selection and limits derived from your own data.

Water & Wastewater Microbiology

Potable, packaged, purified, WFI, process and effluent water testing against IS 10500, IS 14543, WHO and pharmacopoeial limits, with biofilm and distribution system investigation.

Surface & Swab Testing

Hygiene verification and cleaning validation — swabs, contact plates, sponge and rinse sampling with recovery efficiency studies and defensible acceptance limits.

Microbial Contamination Investigation

Structured root cause analysis — organism identification, strain typing, source tracking and harbourage site location, with corrective action and effectiveness verification.

Sterility Testing

Membrane filtration and direct inoculation under USP <71>, Ph. Eur. 2.6.1 and IP for parenterals, ophthalmics, implants and devices, with method suitability and positive-result investigation.

Microbial Limit Testing

TAMC, TYMC and specified organism screening under USP <61> and <62> with acceptance criteria by route of administration, method suitability and objectionable organism assessment.

Bioburden Testing

Pre-sterilisation microbial load under ISO 11737-1 with validated extraction, recovery efficiency correction, sterilisation dose setting support and quarterly monitoring.

Microbial Identification

Identification to genus, species and strain level by Gram stain, biochemical panels, MALDI-TOF, 16S rRNA and ITS sequencing and whole genome typing, with facility flora libraries.

Culture & Sensitivity Testing

Isolation with disc diffusion and MIC determination, disinfectant efficacy validation against your own facility isolates, preservative resistance profiling and rotation programme design.

Shelf-Life & Stability Studies

Real-time and accelerated storage trials, USP <51> preservative efficacy challenge testing, in-use stability and statistical shelf-life modelling for defensible expiry dates.

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