Trainings
Trainings
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- 6-7 June 2024
- Online
Organizations live today, more than ever, in a complex and constantly changing context and this is why flexibility and readiness [...]
Soft Skills
- 10 June 2024
- Online
Conducting clinical trials is a complex activity that involves knowledge of specific standardized documentation and involves multiple stakeholders and different [...]
Clinical Research
NEW
- 10-17 June 2024
- Online
Il corso si propone di illustrare i criteri generali del campionamento in ambito GMP, che devono essere applicati per la [...]
Quality & Process
NEW
- 11 June 2024
- Online
Periodic Safety Update Reports, also called PSURs, are pharmacovigilance documents aimed at providing an assessment of the risk-benefit balance of [...]
Pharmacovigilance
- June 11th 2024
- Online
With the applicability of Regulation (EU) 2017/745, there is a need to review the approach to the preparation of the [...]
Medical Device
- 12 June 2024
- Online
Since October 2015, Annex 15 of the European GMP has been in effect. With this revision, modern process aspects are [...]
Quality & Process
- 12 June 2024
- Online
The objective of the training course "Drugs registration requirements in extra-EU countries" is to illustrate, through practical examples, the registration [...]
Regulatory Affairs
- June 13th 2024
- Online
Observations by inspectors regarding documentation non-compliances are among the most frequent.
The "Documentation Inspection Readiness" training course aims to illustrate, through [...]
Quality & Process
- 13-14 June 2024
- Online
The training course “Time management: optimize your time and reduce stress”, in the era of multitasking, aims to activate changes [...]
Soft Skills
- 14 June 2024
- Online
The training “Preclinical studies in drug registration: focus on toxicology guidelines and CTD structure”, will give an overview of the [...]
Regulatory Affairs
- 17 June 2024
- Online
What is auditing in clinical trials and why is it so important? Conducting clinical trials is a complex activity, that [...]
Clinical Research
- 18 June 2024
- Online
ISO 13485:2016 specifies requirements for a Quality Management System that can be used by an organization in the design, development, [...]
Medical Device