Biograding Establishment

biograding establishment provides complete support in your medical device development. we plan and execute your preclinical trial for ema and fda approvals. in addition to providing routine internal quality maintenance support, biograding establishment has a comprehensive set of standard operating procedures (sop), guidelines, staff training, and regulatory projects, reviews and audits. coupled with the professionalism of our staff all this contributes to maintaining the reputation of biograding establishment for higher quality which: ensures that client’s requirements are met. enables employees to conform to all gcp, glp standards and other regulatory requirements. ensures that all company activities are controlled and documented provides guidance for staff development and training.