Validation Services for Pharmaceutical, Medical Device & Biotech Industries
Being in Compliance is more affordable than being out of Compliance
IQ/OQ/PQ Protocol writing services based on your requirements
IQ/OQ/PQ Performance using highly trained and qualified staff
Wide Range of Validation Services
Autoclaves Ovens Hardness Testers
Disintegrators Friability Testers Stability Chambers
Temperature Mapping and Validation Services
Autoclave Temperature Mapping and Biological Indication Validation
Our engineers design and execute custom protocols to meet your process’s specific load patterns and execution cycle requirements.
Refrigerator, Freezer and Cryogenic Thermal Mapping Qualification – Validation
GMP and GLP storage qualification – validation services. -196°C, -80°C, -20°C or 5°C storage units, custom or template protocols available.
Stability Chamber and Incubator GxP Mapping Qualification. Parameters tested for temperature, humidity and CO2
Custom protocols available, template protocols adhere to International Conference on Harmonization (ICH) conditions: 25°C /60% RH, 30°C /65% RH, 40°C /75% RH, or customer condition.
Oven Temperature Mapping Qualification – Vacuum / Drying / Dehydrogenation
We provide custom protocol development to fit your unique application.
Walk-In Stability Chamber Mapping Qualification – Validation
We provide mapping service for walk-in, controlled cold rooms, GMP warehouses, temporary storage trailers and oversized storage environments.
On-Site Validation Services
We offer on-site validation services for those concerned with equipment down time