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Asphalion @UC3gpnF1gblCOpV_u64tXNCw@youtube.com

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ASPHALION is an international Regulatory, Scientific & Safet


38:14
WEBINAR | “DADI Q&A beyond the Q&A document”
31:20
Webinar: 'ISO IDMP_ how does it change our current processes'
03:31
International Day Women & Girls in Science 2022 at Asphalion
47:39
Veterinary Pharmacovigilance – New Regulation from 28 January 2022
02:23
Asphalion's Highlights: Fourth Quarter 2021
29:01
RegTalks about Regulatory Information Management Systems (RIMS)
48:48
Webinar about EUDAMED MODULE 2
13:51
RegTalks about Regulatory Information Management Systems (RIMS)
38:46
RegTalks about Regulatory Information Management Systems (RIMS)
02:23
Asphalion's Highlights: Third Quarter 2021
59:29
Webinar: “Towards a Smooth Transition to ISO IDMP”
18:19
RegTalks about Regulatory Information Management Systems (RIMS)
09:47
Horizon Europe: New Challenges
10:12
RegTalks "Key factors about the implementation of the new Clinical Trials Information System (CTIS)"
19:20
RegTalks by Asphalion - Horizon Europe: Key aspects to prepare a succesful proposal
02:31
Asphalion's Highlights: Second Quarter 2021
01:12:07
Edited Version - Webinar about US Investigational New Drug (IND) Applications.
01:15:32
Webinar about US Investigational New Drug (IND) Applications
02:31
We are Asphalion
01:01:36
ASPHAFORUM - Covid-19 vaccine safety signal
01:10
Asphalion´s Highlights: First quarter 2021
01:07
Asphalion Pharmacovigilance New Services
48:29
Expedited regulatory pathways
38:27
MDR postponed an opportunity that cannot be missed
57:41
Latest developments of vaccines for COVID-19
41:08
ATMP regulation in EU and FDA
54:22
Product development pathways and strategies for commercialisation of ATMPs
57:08
Introduction to ATMPs: scientific basics and regulatory definitions for newcomers
56:30
Cómo superar una inspección de Farmacovigilancia: puntos clave
59:26
Update in antiretroviral assays against COVID-19
25:29
Post-Marketing Surveillance
36:29
Clinical Evaluation of Medical Devices according to EU MDR 2017 745
49:14
Regulatory issues in emergency situations as COVID-19
30:40
The latest scientific data on the novel coronavirus SARS-CoV-2 and the COVID-19 disease
01:19:43
Medical Devices Webinar by Asphalion
41:21
Bases de datos de Farmacovigilancia ¿qué debe saber IT
01:14
Asphalion Video Corporate
59:23
Challenges of the translation management during and after the CP
43:06
Webinar para administradores_ eSUBmanager - compartir secuencias, ahorrar tiempo y espacio
38:16
eCTDmanager Avanzado - Formación online para administradores
00:54
New office in Barcelona
00:17
#Asphalion is starting a very special 2019
01:16:55
eCTDmanager - Formación online para administradores
00:41
Asphalion at CPhI 2018
39:30
EUDRAVIGILANCE DATA ANALYSIS SYSTEM
00:41
ASPHALION at BIOSPAIN 2018
55:11
Simplifying the Management of Complex SPOR Data
02:31
Asphalion Services
27:54
Aplicación práctica de las actividades regulatorias de serialización en la AEMPS
15:54
Webinar: Medical Literature Monitoring
50:00
Practical Management of Eudravigilance: Case Processing
00:50
ASPHALION in DIA Regulatory Submissions, Information & Document Management Forum
02:00
Asphalion FDA Regulatory Affairs
02:20:19
FDA Regulatory Affairs Webinar - Asphalion
29:07
Implementing the New European Medical Devices Regulations
40:04
Data extraction from SmPCs into structured data for ISO IDMP compliance
54:43
Speed Up Spain - An Approach To Regulatory Procedures In Spain
11:29
Interview of Lidia Canovas from Asphalion at BioSpain 2016