Averica’s chromatography systems contain custom innovations, delivering the fastest turnaround and highest recovery in purification without sacrificing any quality. Upon completion of a project clients receive highly pure compounds, an optimized method, and detailed reporting and analytics.
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.
Averica’s method development services ensure that your team make the best decisions and hit drug development milestones.
We offer a full range of testing and storage services to meet the performance needs of our clients.
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 have two distinct GMP validation departments; chemistry and microbiology. Each validation department is dedicated to development, validation, verification, recovery and inter-laboratory transfer of analytical methods.
We are committed to providing our clients with the highest quality in analytical (chemistry, chromatography, microbioology) services.
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.