We specialize in analytical method development.
Averica provides pharmaceutical development teams with first-class solutions that help them make the best decisions and hit their drug development milestones.
Averica is unique in our approach to impurity isolation, in that we use our scalable separation expertise to isolate significant amounts of unknown chemical impurities.
- Isolation
- Characterization & Profiling
- Structure Elucidation
- Stress/Forced Degradation
- Mass Balance
- Stability Studies
Averica’s method development services ensure that your team make the best decisions and hit drug development milestones.
- Analytical Development
- Chiral
- Release Testing Method
- Stability Indicating Methods
We offer a full range of testing and storage services to meet the performance needs of our clients.
- Qualification of Regulated Starting Materials
- Stability Testing
- EPSA
- pH/Solubility Profiling
- Stress/Forced Degradation
- Mass Balance
- Potency Assays
- Solubility Excipient Screening
- Chiral Release Testing
- Evaluate Limit of Detection (LOD) & Limit of Quantitation (LOQ)
GMP Services
In late 2016, we were acquired by Neopharm Labs Inc. Based in the Montreal area, Neopharm has a 25-year history of excellence in pharmaceutical testing and analysis. In combining the two companies, we’ve developed a fully integrated platform of services capable of taking your program from preclinical stage to commercial launch.
We offer complete microbiology and sterility testing to help ensure the safety of various products and ingredients including pharmaceuticals, cosmetics, personal care products, vitamins, water, veterinary products, natural health products, etc.
We are committed to providing our clients with the highest quality in analytical (chemistry, chromatography, microbiology) services.