Clinical Research

Clinical Research

Training

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  • 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
  • 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
  • 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
  • 20 June 2024
  • Online
Investigational Medicinal Products, or IMPs, are defined as "a pharmaceutical form of an active ingredient or placebo that is tested [...]
Quality & Process
  • 25 June 2024
  • Online
How to manage the audit cycle as a whole? What are the most important aspects to consider? Audit is a time [...]
Clinical Research
  • 25 September 2024
  • 12 March 2025
  • Online
Gli studi osservazionali sono studi il cui protocollo non prevede un intervento diretto del ricercatore nella manipolazione delle variabili oggetto [...]
Clinical Research
NEW
  • 20 November 2024
  • 15 May 2025
  • Online
One of the main priorities of a clinical trial is the safety of the subjects enrolled in it. For this [...]
Clinical Research
  • 27 November 2024
  • 28 February 2025
  • Online

Il 31 gennaio 2022 è entrato in vigore il Regolamento UE 536/2014 (CTR) andando ad abrogare la Direttiva 2001/20/CE (CTD).<br [...]

Clinical Research
NEW
  • 12 December 2024
  • 11 June 2025
  • Online
Conducting clinical trials within the clinical research center includes as a key person the "Investigator," which is the figure who [...]
Clinical Research