ANALYTICAL SERVICES

 
 

Our Analytical Group provides responsible and reliable customized validated testing services in support of drug and cosmetic claims substantiation, verification of active ingredient components (sub potency), product and ingredient stability, new drug applications (NDA) as well as a number of specialized efforts in addressing issues facing the organic and natural products industries.  With the renewed FDA activity involving verification of product claims and substantiation of active and promotional ingredients, we are focusing our efforts on providing the maximum support and expertise to the small to medium entrepreneur operations facing the currently mounting legal and regulatory analytical challenges.

 
 

We provide the maximum support and expertise to small and medium entrepreneur operations facing legal and regulatory analytical challenges.

 
 

USP Validated Testing Services

Titanium Dioxide, Zinc Oxide, Salicylic Acid, Menthol, Camphor, Benzalkonium Chloride, Benzethonium Chloride, Phenxoyethanol Methylparaben, Propylparaben, Octinoxate Octisalate, Oxybenzone, Avobenzone, Homosalate, Hydroquionone, Hydrocortizone, Dimethicone, Petrolatum, Benzocaine, Lidocaine, Benzophenone, Heavy Metals - Lead, Mercury, Cadmium, Arsenic

Analytical Method Development

GC, IR, HPLC

GCMS and LCMS

Specialty Services

Product De-Formulation, New Drug Applications (NDA) Investigational and Analytical Support, Direct Access - FDA Corporate/Product Registration, FDA Sub-Potency Analysis, Methods Development - Product/Active Stability, 6 Month ICH Accelerated Stability, 12 Month ICH Shelf Life Stability