In the late stages of compound discovery, deciding whether to nominate a compound for a full development effort requires a deep understanding of risks and efficacy, potential toxicity, as well as scalability and stability.
As your IND enabling partner, Averica’s services help teams answer the questions that assess the developability of a compound, and ensure that supply of critical assay material is never an issue.
Click the service link to learn the value Averica can provide to your drug discovery and drug development programs.
Chromatography is your best solution for enantiomer supply at the early and intermediate stages of lead candidate profiling. Chiral separation… Read more
Impurity isolation and identification offers you critical information on the structure of your impurity, triggering synthesis efforts that contribute directly to… Read more
Averica Offers HPLC Method Development & Validation Services Our scientists develop analytical methods that are robust, transferable, reproducible, and designed to generate… Read more
Our skilled and competent GMP chemistry group uses a wide range of methods to test raw materials, finished products and packaging… Read more
We offer a full range of stability testing and storage services to meet the performance needs of our clients. Our stability… Read more
We have two distinct GMP validation departments; chemistry and microbiology. Each validation department is dedicated to development, validation, verification, recovery and… Read more
We offer complete microbiology and sterility testing to help ensure the safety of various products and ingredients including pharmaceuticals, cosmetics, personal… Read more
We are committed to providing our clients with the highest quality in analytical (chemistry, chromatography, microbiology), consulting, stability, development and validation services.… Read more