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Core Competencies
Since 2003, PharmOptima's unique approach to drug evaluation and optimization focuses on our ability to maximize the success of your program. We develop customized solutions for your intellectual property problems, and provide the highest quality data in a rapid timeframe. We help our clients select the best candidates to accelerate drug development and increase your chances for clinical success.Founded by scientists with broad expertise and extensive industry experience, we truly understand the value of solving the complex problems associated with drug development programs. Our multi-disciplinary scientific team consults with you to provide research strategies to optimize your success.PharmOptima offers both GLP and non-GLP bioanalytical services, DM and PK, PK/PD, in vivo proof of concept services and consulting.From our quality to our consistency, from our scientific integrity to our project team approach, all our efforts are geared toward providing our customers with what they need,PharmOptima’s Core Expertise
- In vivo ADME, in vitro ADME, qualitative & quantitative analysis, metabolite profiling and GLP bioanalytical method validation plus analysis
- Mass spectrometry (LCMS and GCMS) and pharmacology
- Animal proof of concept testing; experimental formulations for in vivo delivery, PK, and efficacy including ocular PK and non-GLP tolerance
- Experienced in biochemistry and screening
About PharmOptima
- GLP compliant analytical laboratory analyses
- Preclinical PK, PK/PD assessments and ADME for IND submission; additional ADME services for NDA filings
- In vivo model development, pharmacology and PD/PK studies
- Development and validation of analytical assays
- Analysis of compounds in test articles and biological matrices
- Knowledge of the requirements for successful drug discovery and registration
Additional Information
Contact us
Phone: 269-329-4370
