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Zenosis | Pharmaceutical eLearning | Biotechnology eLearning | Zenosis – Learning for Life
clinical,drug,course,introduction,courses,trials,approval,regulatory,zenosis,clinical trials,drug application,clinical trial,clinical practice,regulatory affairs
Zenosis is a web-based library for eLearning Pharmaceutical in the EU & USA. We have an extensive knowledge base to teach Pharmaceutical & Biotechnology Compliance.
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Данные linkpad ( 18 Апреля 2016 ) | |
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Исходящие (внешние) ссылки домена | 197 |
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Внешние ссылки главной страницы ( 3 ) | |
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homepage.net/ | HomePage Media |
Внутренние ссылки главной страницы ( 76 ) | |
/ | Home |
/benefits/ | Benefits of Zenosis |
/courses/ | Courses |
/essentials/ | Introduction & Overview |
/zenosis_regulatory_affairs/ | Introduction & Overview |
/zenosis_clinical_trials/ | Introduction & Overview |
/gmpqaqc/ | Introduction & Overview |
/zenosis_drug_safety_pharmacovigilance/ | Introduction & Overview |
/zenosis_pharmacokinetics_pharmacodynamics/ | Introduction & Overview |
/zenosis_information_communication_technology/ | Introduction & Overview |
/zenosis_medical_devices/ | Introduction & Overview |
/buy/ | Buy Online Course(s) |
/demo/ | Demos |
/catalogue/ | Catalogue |
/news/ | More… |
/new_course_on_medical_devices/ | New course on medical devices |
/new_course_on_good_pharmacoepidemiology_practice/ | New course on Good Pharmacoepidemiology Practice |
/more_zenosis_courses_approved_by_rscfpm_1/ | More Zenosis courses approved by Royal Society of Chemistry and Faculty of Pharmaceutical Medicine |
/generics_and_biosimilars_in_the_usa/ | New courses on generics and biosimilars in the USA |
/new_courses_on_monoclonal_antibodies/ | New courses on monoclonal antibodies |
/new_course_on_21cfr11/ | New course on 21CFR11 |
/new_drug_application_for_marketing_approval_in_the_usa/ | Course update: The New Drug Application (NDA) for Marketing Approval in the USA |
/four_zenosis_courses_approved_by_royal_society_of_chemistry... | Four more Zenosis courses approved by RSC and FPM |
/course_update_introduction_to_ich_good_clinical_practice/ | Course update: Introduction to ICH Good Clinical Practice |
/new_courses_on_pharmacokinetic_and_pharmacodynamic_studies/ | New courses on pharmacokinetic and pharmacodynamic studies |
/urgent_safety_restrictions/ | New course: Urgent Safety Restrictions |
/new_course_capa_in_medicinal_products_manufacture/ | New course: Corrective and Preventive Action (CAPA) in Medicinal Products Manufacture |
/yet_more_zenosis_courses_approved_by_rscfpm/ | Yet more Zenosis courses approved by Royal Society of Chemistry and Faculty of Pharmaceutical Medicine |
/more_zenosis_courses_approved_by_rscfpm/ | More Zenosis courses approved by Royal Society of Chemistry and Faculty of Pharmaceutical Medicine |
/good_manufacturing_practice_in_packaging_medicinal_products... | New course: Good Manufacturing Practice in Packaging Medicinal Products |
/contact/ | Contact Zenosis |
/zenosis_terms/ | Terms & Conditions |
/brands/zenosis/library/zenosis_module_catalogue.pdf | Download Zenosis Catalogue |
pathfinder.zenosis.com/pathfinder/ | What courses do I need? Find courses based on experience or interests |
/ess01/ | ESS01: Essentials of EU and US Regulatory Affairs for Human Medicinal Products |
/ess02/ | ESS02: Essentials of Monoclonal Antibodies |
/gmp01/ | GMP01: An Introduction to Good Manufacturing Practice for Medicinal Products |
/ct07/ | CT07: An Introduction to Clinical Trials and Drug Development |
/ct03/ | CT03: An Introduction to ICH Good Clinical Practice |
/ct04/ | CT04: An Introduction to Clinical Trial Preparation and Design |
/pv03/ | PV03: An Introduction to Drug Safety and Pharmacovigilance |
/sub01/ | SUB01: Orphan Drug Designation in the USA and Europe |
/sub02/ | SUB02: The European Centralised Procedure (CP) |
/sub03/ | SUB03: The Mutual Recognition Procedure (MRP) |
/sub04/ | SUB04: Preparing Submissions in the Common Technical Document (CTD) Format |
/sub05/ | SUB05: Electronic Common Technical Document (eCTD) |
/sub06/ | SUB06: Variations to Marketing Authorisations in Europe |
/sub09/ | SUB09: The New Drug Application (NDA) for Marketing Approval in the USA |
/sub11/ | SUB11: The Decentralised Procedure (DCP) |
/sub12/ | SUB12: Registration of Medicinal Products Based on Monoclonal Antibodies |
/sub13/ | SUB13: How to Gain Approval to Market a Generic Drug in the USA |
/sub14/ | SUB14: The Regulatory Pathway to Licensure of Follow-on Biologics (Biosimilars) in the USA |
/ct01/ | CT01: How to Obtain Approval to Conduct Clinical Trials in Europe |
/ct10/ | CT10: The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials |
/ct06/ | CT06: Clinical Trial Monitoring: Site Evaluation and Setup |
/ct08/ | CT08: Clinical Trial Monitoring: Study Monitoring, Documentation and Closure |
/ct09/ | CT09: Good Clinical Practice Inspections and Audits |
/gmp02/ | GMP02: Good Documentation Practice |
/gmp03/ | GMP03: Good Manufacturing Practice in Cleaning and Sanitation |
/gmp04/ | GMP04: Good Manufacturing Practice for the Warehouse |
/gmp05/ | GMP05: Good Manufacturing Practice in Processing Medicinal Products |
/gmp06/ | GMP06: Good Manufacturing Practice in Packaging Medicinal Products |
/gmp07/ | GMP07: Corrective and Preventive Action (CAPA) in Medicinal Products Manufacture |
/qac01/ | QAC01: An Introduction to Good Quality Control Laboratory Practice |
/pv04/ | PV04: Signal Detection and Management in Pharmacovigilance |
/pv05/ | PV05: Risk Management Planning for Medicinal Products |
/pv06/ | PV06: Urgent Safety Restrictions |
/pv07/ | PV07: Good Pharmacoepidemiology Practice |
/pkpd01/ | PKPD01: An Introduction to Pharmacokinetics and Pharmacodynamics in Drug Development and Registration |
/pkpd02/ | PKPD02: Conducting Pharmacokinetic and Pharmacodynamic Studies |
/ict01/ | ICT01: Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures |
/md01/ | MD01: An Introduction to the Regulation of Medical Devices |
/terms/ | Terms of Use |
/privacy/ | Privacy |
/articles/ | Articles |
/site_map/ | Site Map |
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