NVAK Biotech Instruments
Validation N Decontamination
Customized Validation and Decontamination services as per your requirements
• VALIDATION • DECONTAMINATION •
Validation & Decontamination you can trust for every instrument in your lab.
We deliver end-to-end validation and decontamination services for scientific and pharma equipment—covering risk assessment, protocols, execution, documentation, and audit support.
Request a Validation PlanISO 17025 • 13485 • GMP • 21 CFR Part 11
From single instruments to full facilities—protocols, execution, and documentation aligned with global regulations.
Validaiton for your equipment fitment
Validation of your lab equipments for optimizing their performance.
Validation with reports
Regular validation not only helps maintain compliance but also reduces downtime, prevents data inaccuracies, and extends the lifespan of critical scientific instruments.
Industries & Instruments
Pharma • Biotech • CRO • Food & Beverage • Diagnostics • Research Labs
Biosafety Cabinets
Flow, Precision, Accuracy, Linearity, Carryover.
Laminar Air Flow Cabinets
Clean, Unidirectional Airflow.
Ducted / Ductless Fume Hood
Airflow pattern, Duct integrity, and Containment.
Compliance & Standards
ISO/IEC 17025
Laboratory competence guidance for calibration & testing.
EU GMP / WHO GMP
Validation planning consistent with Annex 15 & GAMP 5 principles.
21 CFR Part 11
Electronic records/signatures and data integrity controls.
How We Work
01
Site ClearanceGet clearance from the site to start validation process.
02
Equipment CleanlinessClean the equipment thoroughly before start of validation.
03
ValidationPerform Validation as per Standard Operating Procedures (SOP).
04
DecontaminationPerform Decontamination for the equipment based on client's request..
Need a quote or site visit?
Share your equipment list and we’ll build a validation plan.