Documents
- b1_02_general_introduction_international_laws.pdf
- b1_03_qms.pdf
- b1_04_inspection_of_your_facility.pdf
- b1_05_disapproved_safety_save.pdf
- b1_07_knowledge_management.pdf
- b1_08_toolbox_improving_organization2.pdf
- b2_09_principles_of_validation_and_qualification.pdf
- b2_11_risk_management.pdf
- b2_12_aseptic_facilities.pdf
- b2_13_media_fills.pdf
- b2_14_aseptic_personnel_qualification.pdf
- b3_1_media_fills.pdf
- b3_2_process_validation.pdf
- b3_3_environmental_monitoring.pdf
- b3_4_cleaning_disinfection.pdf
- culture_presentation.pdf
- dcvmn_ge_rio.pdf
- guidance_for_industry_process_validation_-_general_principles_and_practices.pdf
- ich_q_10_and_beyond_presentation.pdf
- ich_q10.pdf
- picture_vessel_with_liquid.pdf
- picture_graph_sterilisation.pdf
- quality_culture_and_its_measurement.pdf
- rush_dcvmn_july_2015_final_video_link.pdf
- the_training_process.pdf
- vaccine_regulatory_requirements_in_brazil__anvisa_rio_july_10.pdf
- who_good_manufacturing_practices_for_sterile_pharmaceutical_products.pdf
- who_training.pdf
- draft_agenda_v1.pdf
