Planning for Sampling and Analysis of intermediates samples with respect to predetermined specifications and customer requirements (Instrumental&Chemical).
HPLC analysis with respect specifications.
Maintain and perform the calibration of instruments like GC, Analytical Balance, PH meter and KF Titrator.
Maintenance and updating of inward registers and instrument log entries as per the Good Documentation Practices.
Preparation of mobile phases as per standard Testing procedures.
Following Good Laboratory Practices.
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.