- bacteriological and bacterioscopic investigation - quality control - validation of new methods, reagents, test-systems etc. - tranings for lab. staff - SOP development - administration of laboratory information system - participation in audits of technological processes in other labs (used as an autsoursing) and in internal audits (according to ISO) as an auditor - participation in Company's marketing activity

- Written translation of clinical trial protocols, clinical/non-clinical reports, registration dosier, instructions for use (medical equipment, medicines), PSUR etc. - Project management (approx. 1 year)

ICSR collection, review, registration and submission to Health Authorities PSUR/PBRER submission to Health Authorities PV related trainings for staff and 3rd parties

- registration and processing of biological samples, - data entering - execution of laboratory tests (ELISA and protein electrophoresis)

- communication with CRO and pharmaceutical companies - management of clinical trial projects (central laboratory services) - trainings for laboratory staff and for Investigators (participation of investigator meetigs) - document development (Laboratory manuals, SOP etc.) - participation in audits

- communication with investigators, courier service, warehouse. - data entry into the database, - preliminary protocol work