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Non-clinical study planning for biocompatibility
Clinical evaluation reports (CERs) preparation
Post-market clinical follow-up (PMCF) planning
Clinical trial protocol development
Bioequivalence study design
Pharmacokinetic and pharmacodynamic study planning
Nonclinical toxicology program planning
Clinical study design for efficacy claims
Safety studies for novel ingredients
Bioavailability and absorption studies
Literature review and gap analysis for claim substantiation
Challenge studies for food safety
Shelf-life studies design and management
Sensory evaluation studies
Nutritional analysis studies
Safety assessment studies for cosmetic ingredients
Dermal absorption studies
Sensitization and irritation testing strategies
Efficacy studies for cosmetic claims