We provide services from Visakhapatnam facility in India. A highly qualified and experienced team of professionals work...
FDA approved State-of-the-art facilities with access to 138 beds.
Excellent scientific and clinical expertise with capabilities of handling challenging studies.
Successful inspections by USFDA for all Actimus Bio facilities.
Our team comprising of professionals equipped with Clinical Trial Management expertise We have amassed...
Actimus Bio has a dedicated team experienced with over 1000+ Clinical studies ranging from BA/BE to Human Pharmacology...
Our medical writing services include Publication Writing, Regulatory Writing, Safety Documents, and Medical...
Accurate, accessible and reproducible high quality data State-of-the-art technologies compliant...
Any pharmaceutical product manufacturer requires a quality control, which is one of the Pre- requisite to regulatory compliances.