e.alvarado2022-08-04T13:34:30+00:00August 3rd, 2022|Categories: AboutPharma|
Gli attacchi informatici possono paralizzare il funzionamento dei sistemi in qualsiasi settore. Tuttavia, nel caso dell’assistenza sanitaria, tale paralisi può essere una questione di vita o di morte. Di recente, la sicurezza dei dispositivi medici è diventata [...]
e.alvarado2022-08-04T13:36:16+00:00August 3rd, 2022|Categories: Meditrial|
Cyber attacks can cripple the operation of systems in any sector. However, in the case of health care, such paralysis can be a matter of life and death. Recently, medical device security has become a global concern and a [...]
e.alvarado2022-08-04T13:38:16+00:00July 27th, 2022|Categories: AboutPharma|
La sanità è connessa a ogni aspetto della società. Ci affidiamo a medici altamente qualificati per mantenerci in salute utilizzando la loro vasta conoscenza e strumenti e risorse cliniche progressivamente più avanzati. Ma i medici di tutto [...]
e.alvarado2022-08-04T13:42:31+00:00July 27th, 2022|Categories: Medical Research, Meditrial|
Health care is connected to every aspect of society. We rely on highly qualified physicians to keep us healthy by using their vast knowledge and progressively more advanced clinical tools and resources. But physicians around the world involved in [...]
e.alvarado2022-08-04T13:43:59+00:00July 20th, 2022|Categories: Medical Research, Meditrial|Tags: Case Report Design, Clinical, Clinical Data Management Practices, Clinical Data Management Software, Data Management, Serious Adverse Events, SOPs, Study Setup|
When novel drugs or medical devices are evaluated in clinical trials, the data generated in this process is called clinical data. Improving the use of technology in clinical trials is now a prime opportunity for the life sciences industry. [...]
adminMTE_04792022-08-04T13:48:07+00:00July 20th, 2022|Categories: AboutPharma|
Quando i nuovi farmaci o i dispositivi medici sono valutati nell'ambito degli studi clinici, i dati generati in questo processo sono definiti dati clinici. Oggi migliorare l’utilizzo della tecnologia negli studi clinici è un’esigenza primaria per il [...]
e.alvarado2022-08-04T14:05:47+00:00July 6th, 2022|Categories: Meditrial|Tags: Clinical Trial, Estimand, ICH, PRO, Study Planning|
Edited by Dr. Monica Tocchi, Meditrial medical director. The organization called ICH (International council for harmonization of technical requirements for pharmaceuticals for human use) is a global organization that unites regulatory authorities and the pharmaceutical industry in the common [...]
adminMTE_04792022-08-04T14:07:45+00:00July 6th, 2022|Categories: AboutPharma|
A cura di Dr. Monica Tocchi, direttore medico Meditrial. L’organizzazione chiamata ICH (International council for harmonisation of technical requirements for pharmaceuticals for human use) è un’organizzazione globale che unisce le autorità regolatorie e l’industria farmaceutica nell’obiettivo comune di [...]
e.alvarado2022-08-04T14:21:10+00:00June 28th, 2022|Categories: Meditrial|Tags: Clinical Trial, Devices, GCP, Good Clinical Practice, IN-VITRO, IVD, IVDR, Medical Devices|
Atty. Alessia Nuciari, director of compliance Meditrial. The in vitro diagnostics industry has undergone a substantial transformation. IVDR Regulation 746/2017, published in May 2017 and applied from May 26, 2022, introduced major changes in the industry. The main [...]
adminMTE_04792022-08-04T14:11:33+00:00June 28th, 2022|Categories: AboutPharma|
Avv. Alessia Nuciari, direttore responsabile Compliance Meditrial. L'industria della diagnostica in vitro ha subito una trasformazione sostanziale. Il Regolamento IVDR 746/2017, pubblicato a maggio del 2017 e applicato dal 26 maggio 2022, ha introdotto importanti cambiamenti [...]
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