Sipra Labs Limited is a global contract research organization offering end to end regulatory compliant research and developmental services to the Pharmaceutical, Biotech and Medical Devices industries for two decades. Sipra has supported many global and indigenous pharmaceutical players for their dossier submissions to highly regulated markets like the US, Europe and Japan.
Sipra is having 24 years of immense experience in Product Design, Development, Testing, Validation, Dossier Preparation, Registration and Post-marketing studies i.e., End to End.