+91 9744122269 contact@precore.in
We take up turnkey project consultancy and execution in following Life science areas
Our project engineers will handle the project from its design phase to validation and commissioning. We make facilities meeting all regulatory requirements in par with US FDA. Our cost effective solutions bring downs your budget of facility construction to more than 40%.
We do customized automation projects for Laboratories, Medical device/Pharmaceutical manufacturing facilities and Healthcare establishments.
We facilitate technology Transfer for In vitro Diagnostics manufacturing
Precore offers complete regulatory assistance for registration and certification of medical devices. Our consultancy service is offered for regulatory approvals from CDSCO and state FDA, ISO 13485 and GMP audits. Our service include,
Complete documentation work as per MD/IVD guidelines , Technical Documentation work for all regulatory approvals, ISO 13485 implementation, Regulatory Consultancy and documentation, Complete regulatory approval for Manufacturing Facility, test License and Product Approval, Validation of plant and process, Training of Staff for QMS and GMP
