Training Seminars

In this section you will find all training courses organised by AICRO and aimed at
to develop professional skills and competences
in the field of Clinical Research

2023

27/06/2023 WORKSHOP: IMPLEMENTATION OF THE EU REGULATION ON CLINICAL TRIALS IN ITALY: COMPARING EXPERIENCES

Posted by aicro
On 21 June 2023
0 Comments

AICRO, in collaboration with the Department of Integrated Activities Research and Innovation (DAIRI) organises the workshop entitled: APPLICATION OF THE EU REGULATION ON CLINICAL TRIALS IN ITALY: COMPARING EXPERIENCES Tuesday, 27 June 2023 10:00 – 13:00 Representation Hall of the Azienda Ospedaliera SS Antonio e Biagio e C. Arrigo of Alessandria Via Venezia, 16 Alessandria […]

2021

21 AND 22 OCTOBER 2021: PHARMACOVIGILANCE IN CLINICAL TRIALS

Posted by aicro
On 10 June 2021
0 Comments

21 AND 22 OCTOBER 2021: PHARMACOVIGILANCE IN CLINICAL TRIALS: common assessment tools, promoter responsibility, where to optimise activity 1st Module – 21 October 2021 15:00 – 18:00: Pharmacovigilance in Clinical Trials 2nd Module – 22 October 2021 14:00 – 16:30: Focus on surveillance in clinical trials with medical devices AICRO organizes a seminar with focus […]

24 September 2021: Remote monitoring

Posted by admin
On 7 June 2021
0 Comments

Remote monitoring: real life experiences Webinar – 24 September 2021 – 9:00 – 11:30 am Remote monitoring is a very topical subject and the experience of the recent pandemic has accelerated its development and highlighted its potential. AICRO will share experiences, critical issues and solutions through the testimonies of its members, who are daily engaged […]

2020

25 June 2020: The concept of “vigilance” in clinical trials expands the boundaries

Posted by admin
On 22 May 2020
0 Comments

from drug experience to medical device. The normative background, language and modes of action: comparing experiences An interactive seminar, albeit in webinar mode, during which we will go through the requirements of pharmacovigilance in clinical trials in brief pills, and then hook the imminent need to adapt the activity of "vigilance" also to the medical device. The speakers will refer to the current regulations, and then share with the participants direct experiences and offer a multi-faceted panorama faced by different actors: the CRO, the Sponsor, the CTC in support of independent research [...]

2019

10 OCTOBER 2019: “The production of the drug for experimental use”

Posted by admin
On 5 August 2019
0 Comments

Regulation: the EudraLex vol. 4 GMP - Annex 13 reference legislation Activities related to the preparation of the IMP, description of the process: The incoming material; Primary packaging: production of capsules, inflation, blistering; Secondary packaging: MLAF and labelling[...]

25 June 2019: BASIC PHARMACOVIGILANCE

Posted by admin
On 23 April 2019
0 Comments

Basic Pharmacovigilance in Clinical Trials: common evaluation tools, the responsibility of the promoter An interactive seminar during which participants will be able to have a regulatory update on current pharmacovigilance obligations in the field of clinical research and an interaction with specialized professionals in the sector, belonging both to the hospital and to the corporate world, with the aim to verify the common tools available to correctly evaluate the PV activities necessary to conduct a clinical trial[...]

2018

7 June 2018: THE ROLE OF THE CLINICAL PROJECT MANAGER IN THE CRO

Posted by admin
On 7 June 2018
0 Comments

Speakers: – Gabriella Laurora -Director, Clinical Team Management – Chiara Teruzzi – Associate Director, Clinical Team Management – PRA Health Sciences Target: An interactive workshop during which participants will be able to work on cases and will address the following topics: Definition of Clinical Project Manager Competences of the Clinical Project Manager Operational supervision Competences […]

18 April 2018: THE PRODUCTION OF THE DRUG FOR EXPERIMENTAL USE

Posted by admin
On 13 March 2018
0 Comments

Speakers: – Marina Farina (Workshop and QP Manager) – Stefano Busti (Manufacturing Manager) – Deborah Mansalvi (QAM) – Lara Felici (QCM) – Andrea Mazzini (Supplier Specialist) Topics: Regulation: the EudraLex vol. 4 GMP – Annex 13 reference legislation Activities related to the preparation of the IMP, description of the process: The incoming material; Primary packaging: […]

16 March 2018: INFORMED CONSENT

Posted by admin
On 8 August 2017
0 Comments

Speakers: Simona Cimbro, Sr Manager Clinical Monitoring Stefano Gregoriani, Sr Director Country Operations – Chiltern International The following topics will be covered during the course: General considerations Ownership Requirements for validity of information and consent Mode of expression (written consent) Consent in vulnerable patients Minors Incapable and psychiatric patients Seniors State of need and […]

2017

7 April 2017: Post Authorisation Safety Studies

Posted by admin
On 22 August 2017
0 Comments

Speaker: Giovanni Fiori, Scientific Director MediNeos Observational Research The following topics will be covered during the course: Definition of PASS Legal framework Methodological aspects Data collection Data management[...]

13 April 2017: TRAINING FOR MEMBERS

Posted by admin
On 21 August 2017
0 Comments

"European Data Protection Regulation - the impact on the activities of CROs". The purpose of the meeting is to offer participants an update of the legal framework in relation to the European Regulation 2016/679/EU on the protection of personal data.

9 May 2017: INTERNATIONAL PAEDIATRIC CLINICAL TRIAL DAY 2017

Posted by admin
On 20 August 2017
0 Comments

“Helping children create lives they deserve” This year AICRO organizes a Paediatric Clinical Day together with Ospedale San Raffaele, TEDDY and INCiPiT. TEDDY (the European Network of Excellence for Paediatric Clinical Research) is an independent multidisciplinary and multinational research Network, composed by 48 partners from 19 EU and non-EU countries aimed at facilitating the performance […]

28 September 2017: The flow of the experimental drug

Posted by admin
On 18 August 2017
0 Comments

“The flow of the experimental drug: What’s going on behind the scenes” Proper management of the experimental drug increasingly contributes to ensuring the quality of data obtained during a clinical trial. In this context, the flow of the drug between doctor and patient is well known and described while the upstream and downstream stages are […]

22 June 2017: The Clinical Project Manager

Posted by admin
On 18 August 2017
0 Comments

“The role of the Clinical Project Manager in the CRO” An interactive workshop during which participants will be able to work on the cases and will address the following topics: Definition of Clinical Project Manager Competences of the Clinical Project Manager Operational Supervision Financial management Resource management Speakers: – Gabriella Laurora – Director, Clinical Team […]

Training

Training Seminars

In this section you will find all training courses organised by AICRO and aimed at to develop professional skills and competences in the field of Clinical Research

In this section you will find all training courses organised by AICRO and aimed at
to develop professional skills and competences
in the field of Clinical Research