Testing - Keyport, NJ - Loricon Testing

Analyses for analytical testing are performed using approved validated methods. Methods can be transferred from clients or developed and validated in-house. Analytical techniques are conducted by experienced scientists using accepted industry and scientific protocols.

Regulatory Services (Partial List)

Method Development
Method Transfer
Method Validation, includes the following:
- Accuracy
- Precision
- Specificity/Selectivity
- Limit of detection
- Limit of Quantitation
- Linearity
- Range
- Forced degredation can be performed if required by the client.
Compatibility Testing
Cosmetic Stability Testing (non-OTC)
3 month accelerated Drug Stability
Ongoing shelf life OTC Drug Stability at room temperature
Equipment Validation IQ, OQ, PQ
Equipment Cleaning Validation
EU Ingredient Verification
Period After Opening
Stability Storage and Testing
Water Validation
Yearly Bath monitoring

Partial List of Ingredients Tested:

Avobenzone
DMDM Hydatoin
Homosalate
Imidazolidinyl Urea
Kathon CG
Octocrylene
Octinoxate (Octyl Methoxycinnamtate)
Octisalate (Octyl Salicylate)
Oxybenzone
Padimate O
Parabens
PCMX
Phenyl benzimidazole sulfonic acid
Salicylic Acid
Titanium Dioxide
Triclosan
Zinc Oxide

Analytical Laboratory Testing

Active Testing
Batch Analysis
Finished Goods Analysis
Formula Breakdown
Ingredient Verification
Preservative Verification
Product Formulation
Raw Material Activity & Identification
Unknown ID
USP Testing