Isolator Validation
Comprehensive Validation for Optimal Sterility and Contamination Prevention in Pharmaceutical Isolators
Isolator validation ensures sterility and safety by maintaining positive pressure and filtered air, adhering to stringent international standards for pharmaceutical manufacturing environments. It supports efficient, contamination-free operations
Containment Consultancy
Ensuring Safe Handling of Hazardous Materials with Comprehensive Containment
We specializes in designing customized containment systems to prevent cross-contamination, safeguard personnel, and ensure regulatory compliance. Their expertise ensures operational efficiency in pharmaceutical and biotech facilities.
Tech Transfer
Advanced Solutions for Efficient Pharmaceutical and Biotech Process Transition
Technology transfer streamlines the adoption of innovative processes, ensuring safety, compliance, and scalability for pharmaceutical and biotech production needs
Cleanroom Area Validation
Comprehensive Validation for Ensuring Cleanroom Compliance and Maintaining Controlled Environments in Critical Applications
Cleanroom validation ensures controlled environments meet ISO and GMP standards, safeguarding product quality, preventing contamination, and supporting compliance for pharmaceutical and biotech applications.
Occupational Exposure Level Validation
Ensuring Safe Handling of Hazardous Materials Through Comprehensive OEB Level Validation
OEB Level Validation evaluates and categorizes substances based on toxicity, exposure limits, and potency. It establishes tailored containment solutions and protective measures to minimize risks in workplace environments
Contact Details
India (factory- headoffice)