Objectives and competences
The postgraduate course in Quality Systems in the Pharmaceutical Industry and Pharmaceutical Research prepares students to develop a unique integrated quality system to comply with European and international regulations, such as Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) and Good Clinical Practices (GCP), the ISO, the ICH and FDA guides and pharmacovigilance regulations, among others. The course provides professional skills and knowledge to be an expert in pharmaceutical quality.
Basic information
| Type | Postgraduate courses |
|---|---|
| Certificate | Specialization diploma |
| Faculty or school | Institut de Formació Contínua IL3 |
| Branch of knowledge |
|
| Mode of delivery | Distance |
| Credits | 30 |
| Length of course | 1 academic year |
| Language(s) of instruction | Spanish |
| Enrolment fee: | First year: 3.680,00 € An increase of 10% is applied to the price, up to a maximum of € 70, as administration fee |
| In-company placement(s): | No |
| Classes begin: | 08/04/2024 |
| info@il3.ub.edu | |
| Master's degree course homepage | http://www.il3.ub.edu/ca/postgrau/postgrau-sistemes-qualitat-industria-recerca-farmaceutica.html |
| Managment | Ribó Ros, Cristina |
| Open pre-enrolment | No |
| Lead to doctoral studies | No |
| Admission for applicants not holding a degree qualification: | Sí, amb crèdits pendents (10% o menys) |
Objectives and competences
Objectives
- To learn useful tools to design a quality system that is flexible to adapt to the new regulations and contains elements that maximise efficiency and reduce the costs of quality systems. This reduces the risk of problems derived from inadequate quality systems, such as complaints, corrective actions, etc.
Specific objectives:
- To be able to integrate different regulations and quality systems to achieve operational excellence.
- Manage all records, protocols and reports relating to quality in the pharmaceutical industry, research centres, biotech companies, etc.
- Supervise and assess the supply chain; that is, the products and subcontracted services.
- To identify possible sources of non-compliance or risk, to guarantee successful audit results and prevent complaints or corrective action.
Access and admission
Applicant profile and access requirements
Recommended applicant profile
- Professionals working in the pharmaceutical and biohealth industry; particularly those in quality control and assurance, pharmacovigilance, validations and other areas relating to quality systems.- Professionals in pharmaceutical laboratories and pharmaceutical research, clinical trials, drug development and analytical development
- University graduates interested in working professionally in this field and related areas.
Access requirements and conditions
The course is also open to students with no prior university education, who will acquire the same knowledge and skills and receive a specific qualification for their learner group. Information on the access requirements and other conditions can be obtained from the course directors.Pre-enrolment
Contact us
Faculty or school where the course is taught
| Address: | Institut de Formació Contínua - UB C/ Ciutat de Granada, 131 08018 - Barcelona Espanya |
|---|---|
| Email address: | info@il3.ub.edu |
| Webpage: | http://www.il3.ub.edu |
| Telephone: | 93 403 96 96 |
| Observations: | 30 hours of videoconference sessions distributed throughout the modules (according to the syllabus), Friday (and occasionally Thursday) from 6 p.m. (in sessions of no more than 1.30 h / except one of 1.45 h. Compulsory attendance of 80% of the sessions. |
For further enquiries
| Address: | Institut de Formació Contínua - UB C/ Ciutat de Granada 131 08018 - Barcelona Espanya |
|---|---|
| Email address: | info@il3.ub.edu |
| Webpage: | http://www.il3.ub.edu/ca/postgrau/postgrau-sistemes-qualitat-industria-recerca-farmaceutica.html |
| Telephone: | 93 309 36 54 |
| Observations: | Monday to Friday, from 9 a.m. to 7 p.m. |