We provide services from Visakhapatnam facility in India. A highly qualified and experienced team of professionals work round the clock and have helped accumulate an expansive assay catalogue of more than 120 validated methods.
Our laboratory is compliant with GLP and equipped with cutting edge, highly sophisticated instruments such as LC-MS/MS (10+ machines which includes API6500, API5500, API4500).
With over 140 validated methods and constantly working on methods at various stages of development at any given point of time, Actimus is perfectly geared up to handle your bioanalytical requirements. Actimus’ bioanalytical experts are capable of developing and validating new methods in a time span of approximately 04-06 weeks. We have experience in undertaking bioanalysis for Preclinical/Toxicity studies,Veterinary generics as per CVM/ANADA requirements. We are proud to state that a large part of our scientists of this team have a wealth of experience that enables us to successfully develop and validate even the most challenging methods.
Samples are stored in controlled and monitored low temperature storage ranging from -25°C, -70°C. Actimus freezers have a capacity to store larger number of samples. A dedicated walk-in chamber of -20°C is available to store the samples until regulatory approval.
Our vast expertise and in-depth understanding of stringent regulatory requirements ensure each project is accomplished in rapid turn-around times. We are proud to be a partner for several prominent generic pharma companies and have helped contribute to their aggressive First To File (FTF) projects timelines by speedy bioanalysis in line with their requirements.
We have also successfully cleared regulatory inspections from FDA. Our Method Validation SOPs are in compliance with all regulatory requirements.
Our enthusiastic BA scientists regularly attend several major bioanalytical workshops and conferences held during the year to keep themselves abreast with the latest in this field.