Training for Quality, Environment, Safety, Ethics, Gmp
A.Y. 2019/2020
Learning objectives
Aim of the course is to provide information on the following relevant aspects of the pharmaceutical field: Quality and Environmental Management Systems, Health and Safety Management Systems, Ethic issues in pre-clinical and clinical development of drugs, Good Manufacturing Practice for pharmaceutical products.
Expected learning outcomes
Ability to work in a ISO9001 Quality management context;
Ability to work in a ISO14001 Environmental management context;
Knowledge of current regulations on workplace Health and Safety system;
Knowledge of current regulations on animal and human studies;
Ability to work according to Good Manufacturing Practices.
Ability to work in a ISO14001 Environmental management context;
Knowledge of current regulations on workplace Health and Safety system;
Knowledge of current regulations on animal and human studies;
Ability to work according to Good Manufacturing Practices.
Lesson period: First semester
Assessment methods: Esame
Assessment result: voto verbalizzato in trentesimi
Single course
This course cannot be attended as a single course. Please check our list of single courses to find the ones available for enrolment.
Course syllabus and organization
Single session
Responsible
Lesson period
First semester
Course syllabus
1) Quality Management System according to ISO9001 standard
Principles and implementation strategies of the standard, providing examples from laboratories of clinical chemistry.
2) Ethical issues in drug development
Steps of Drug development process, key principles for ethical conduct and current national and international regulations.
3) Good Manufacturing Practice (GMP)
Basic requirements for the manufacturing of medicinal products for humans and animals according to GMP and current international regulations.
4) Health and Safety Systems
Basic processes and figures of health and safety protection system at workplace.
5) Risk assessment
Basic processes for risk assessment and management starting from the chemical and toxicological profiles of substances.
6) Environmental Management System
Principles and implementation strategies of the ISO 14001 standard for the reduction of environmental impact.
Principles and implementation strategies of the standard, providing examples from laboratories of clinical chemistry.
2) Ethical issues in drug development
Steps of Drug development process, key principles for ethical conduct and current national and international regulations.
3) Good Manufacturing Practice (GMP)
Basic requirements for the manufacturing of medicinal products for humans and animals according to GMP and current international regulations.
4) Health and Safety Systems
Basic processes and figures of health and safety protection system at workplace.
5) Risk assessment
Basic processes for risk assessment and management starting from the chemical and toxicological profiles of substances.
6) Environmental Management System
Principles and implementation strategies of the ISO 14001 standard for the reduction of environmental impact.
Prerequisites for admission
None.
Teaching methods
Lessons and workgroups.
Teaching Resources
Educational material is available on Ariel website.
Assessment methods and Criteria
Oral exam; questions are aimed to verify the student's knowledge on the course's topics. In itinere tests will not be performed.
BIO/14 - PHARMACOLOGY - University credits: 4
Lessons: 32 hours
Professor:
Gomaraschi Monica
Shifts:
-
Professor:
Gomaraschi MonicaProfessor(s)
Reception:
By appointment
Centro E. Grossi Paoletti, Ospedale Niguarda, Piazza Ospedale Maggiore 3