training

SAVE THE DATE- AICRO – Milan, November 12th, 2015

On November 12th, 2015 the Italian Association Contract Reseach Organisation (AICRO) will organise in Milan (Hotel Principe di Savoia) the event entitled Le “sfumature” della ricerca clinica in Italia, an entirely day dedicated to the clinical research that will address issues on the evolving of new ways of managing clinical trials in Europe (and specifically in Italy), including the synergies between AICRO and clinical trial centres. […]

2017-01-03T11:18:06+00:00 14/10/2015|Categories: News & Events|Tags: , , |

Clinical monitor training course

Bioikòs Farma in collaboration with Consorzio per Valutazioni Biologiche e Farmacologiche (CVBF), CME Provider n. 1053, is pleased to present the thirteenth edition of the course for clinical monitors, which since this year, provides also with Italian CME credits. The course is aimed at young graduates interested in learning about this job profile and professionals who already work in public research institutions such as IRCCS, hospitals, polyclinics or scientific sssociations as researchers, data managers, study coordinator and willing to learn more about the clinical research and the figure of the monitor. The clinical monitor, in fact, is a strategic figure in the context of the clinical trial as he plays a checking role of the validity of data obtained from clinical trials. The course consists of 40-hour lesson (face to face lessons and interactive workgroups) and applies for 50 Italian CME credits. Deadline for applications: 27/02/2015 Please see the following references (ITA) for more information: course brochure course program and calendar registration form For further information, please contact Silvia Smaia at [email protected] o visit the dedicated website.

“G. Benzi” Biennial Master’s Program in Regulatory Sciences

The University of Pavia has launched the eleventh edition of the “G. Benzi” Biennial II level Master’s Program in Regulatory Science. The deadline for the submission of applications is January 15th, 2015. Please see the following references (ITA) for more information: Call for applications to the University of Pavia master’s programs Regulatory Sciences Master’s Program call for applications Master’s Program’s website Master’s Program’s brochure […]

2015-11-26T17:00:57+00:00 05/12/2014|Categories: News & Events|Tags: , , , |

E-learning course “Authorisation procedures for multi-centre and multi-national trials”

The Consorzio per Valutazioni Biologiche e Farmacologiche (CVBF) and the Gianni Benzi Pharmacological Research Foundation (FGB) are pleased to inform you that applications are now open for the new e-learning course entitled “Authorisation procedures for multi-centre and multi-national trials”. The course is free of charge upon registration! It is aimed at providing a guide on the procedures to be followed for the application of clinical trials with medicinal products for human use to the competent bodies to all the involved stakeholders, in the specific case of multi-center and multi-national trials. The Course is available on the e-learning platform CVBF-FGB and consists of 7-hour lesson structured in 5 modules. Each module is constituted by a PowerPoint presentation supported by audio comments and research material (scientific articles, videos, textbook which is a pdf file with the explanation of each slide. All materials can be viewed online or saved by the user on their own computer. The course applies for 10,5 Italian ECM credits for all healthcare professionals, including biologists, pharmacists and physicians. For further information please visit our e-learning platform or contact us at [email protected]

E-learning course “Marketing a drug for human use in Europe”

The Consorzio per Valutazioni Biologiche e Farmacologiche (CVBF) and the Gianni Benzi Pharmacological Research Foundation (FGB) are pleased to inform you that applications are now open for the new e-learning course entitled “Marketing a drug for human use in Europe”. The course is free of charge upon registration! It deals with the procedures to be followed in order to obtain a Marketing Authorisation for medicinal products for human use according to European rules, with particular focus on: Advanced Therapies Medicinal Products (ATMPs) Orphan drugs Paediatric medicines The Course is available on the e-learning platform CVBF-FGB and consists of 8-hour lesson structured in 4 modules. Each module is constituted by a PowerPoint presentation supported by audio comments and research material (scientific articles, videos, textbook which is a pdf file with the explanation of each slide. All materials can be viewed online or saved by the user on their own computer. The course applies for 12 Italian ECM credits for all healthcare professionals, including biologists, pharmacists and physicians. For further information please visit our e-learning platform or contact us at [email protected]

Applications for the International Master of Science in Paediatric Medicines Development and Evaluation now open

The International Master of Science in Paediatric Medicines Development and Evaluation awarded by the University of Rome “Tor Vergata” School of Paediatrics in collaboration with the Children’s Hospital Bambino Gesù and the EU Project Global Research in Paediatrics (GRiP) is now open for registration. […]

2015-11-26T16:39:41+00:00 15/10/2014|Categories: News & Events|Tags: , , , |