Services Offered
- Package Validation
- Biological and Chemical Validation
- Transportation Validation
- Residual Validation
- Particulates Validation
- Environmental Validation
- Sterility Validation
- Method Development and Validation
- Production Process Validation
- Small Molecule Identification and Purity Validation
The Taryag Integrated Approach
By providing medical device and pharmaceutical innovators with an end-to-end development infrastructure that integrates sterilization, validation, packaging, manufacturing, and laboratory services, we help our clients overcome barriers and reduce costs: accelerating their time to market.
Why Choose Taryag?
Providers of transportation testing
Product-oriented sterilization validation
Extensive validation experience with regulatory entities (ISO, FDA, ETC.)
Our Work Process
Receiving Client Specifications And Requirements (Contract Review)
Determining Microbial And Chemical Performance Qualification Protocol
Determining Sterilization Performance Qualification Protocol
Bioburden Testing
Microbial And Chemical Performance Qualification Report Is Prepared
Sterilization Performance Qualification Report Is Prepared
The Final Report Is Produced
Our Environmental Validation Process
Receiving Client Specifications And Requirements (Contract Review)
Protocol Design
Sterilization
Transportation Simulation
Accelerated Aging
Microbial Barrier Testing
Initial Report Is Produced
Real-Time Storage
Microbial Barrier Testing
Final Report Is Produced
Credentials:
