all the past

Courses

for Pharmaceutical and Medical Devices Professionals

Courses found: 31
Order by
WEBINAR GRATUITO: Omero Insegna la Gestione delle Crisi
31 Marzo 2020 ore 11.00
Webinar gratuito

WEBINAR GRATUITO: Omero Insegna la Gestione delle Crisi

Come i capi degli Achei affrontano la peste nel primo libro dell’Iliade

WEBINAR: Clinical Study Report e Clinical Investigation Report
01 Aprile 2020 ore 11.30
Webinar

WEBINAR: Clinical Study Report e Clinical Investigation Report

Un’introduzione sulle similitudini e differenze tra CSR e CIR

WEBINAR: Attributability in Pharmacovigilance, Still a Hot Topic
2 April 2020 at 11 am
Webinar

WEBINAR: Attributability in Pharmacovigilance, Still a Hot Topic

How to navigate the different algorithms and approaches used to evaluate the causality of an adverse event/reaction

WEBINAR: Gli Ostacoli alla Trasparenza dei Dati Scientifici e Come Superarli
03 Aprile 2020 ore 11.30
Webinar

WEBINAR: Gli Ostacoli alla Trasparenza dei Dati Scientifici e Come Superarli

Quali sono le richieste di trasparenza sui dati provenienti dagli studi clinici, quali gli ostacoli alla loro divulgazione e le possibili soluzioni

WEBINAR: Beyond PubMed
7 April 2020 at 2.00 pm
Webinar

WEBINAR: Beyond PubMed

Additional approaches and sources for cost-effective literature monitoring

WEBINAR: Le Risorse Soft nel Project Management
08 Aprile 2020 ore 14.30
Webinar

WEBINAR: Le Risorse Soft nel Project Management

Come ottenere risultati tramite le persone

WEBINAR: Natural Language Processing (NLP) and Text Mining: a Help in Daily Pharmacovigilance Activities
15 April 2020 at 11.00 am
Webinar

WEBINAR: Natural Language Processing (NLP) and Text Mining: a Help in Daily Pharmacovigilance Activities

How to exploit “machine aided” technologies to increase the effectiveness of Pharmacovigilance procedures

WEBINAR: Data Transparency in Clinical Research
16 April 2020 at 11.30 am
Webinar

WEBINAR: Data Transparency in Clinical Research

The obstacles to data transparency and how to overcome them

WEBINAR: Disruptions and Protocol Deviations in Clinical Trials during the COVID-19 Pandemic
29 April 2020 at 11.30 am
Webinar

WEBINAR: Disruptions and Protocol Deviations in Clinical Trials during the COVID-19 Pandemic


WEBINAR: GDPR, Its Impact on Clinical Research Before, During and After the COVID-19 Pandemic
5 May 2020 at 2.30 pm
Webinar

WEBINAR: GDPR, Its Impact on Clinical Research Before, During and After the COVID-19 Pandemic


WEBINAR: Gli Strumenti Statistici per Pianificare e Comprendere Uno Studio Clinico
22-29 April, 06 May 2020
Webinar

WEBINAR: Gli Strumenti Statistici per Pianificare e Comprendere Uno Studio Clinico


Quality Risk Management – Workshop
13 May 2020
Milan

Quality Risk Management – Workshop

A definition of the risk management process in clinical research

WEBINAR: From Theory to Practice: Data Integrity
5-7-12-14 May 2020
Webinar

WEBINAR: From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

WEBINAR: Real-World Data and Real-World Evidence
6-8-12-14 May 2020
Webinar

WEBINAR: Real-World Data and Real-World Evidence

An intensive Webinar to learn the main concepts behind Real-World Evidence and Observational Research and to design innovative studies that generate evidence

WEBINAR: Biomedical Literature, Databases and Bibliometric Indicators
13-19-21 May 2020
Webinar

WEBINAR: Biomedical Literature, Databases and Bibliometric Indicators

Where and how to get the scientific literature that makes the difference

WEBINAR: Promotion of a Pharmaceutical Brand
21-28 May, 04 June 2020 at 10:30 am
Webinar

WEBINAR: Promotion of a Pharmaceutical Brand

Implementing new and traditional pharma promotion channels in accordance to regulations in place

ONLINE TRAINING: The Strategic Role of the Medical Science Liaison during a Product’s Life Cycle
18-20-27 May, 10 June 2020
Online

ONLINE TRAINING: The Strategic Role of the Medical Science Liaison during a Product’s Life Cycle

Four modules training to learn and experience the role of a MSL

WEBINAR: Medical Devices Registration at an International Level
3 - 4 - 10 June 2020
Webinar

WEBINAR: Medical Devices Registration at an International Level

Regulatory strategy and steps for medical device market access with an eye on the Americas, the Asian pacific Region and China

ONLINE TRAINING: General Data Protection Regulation (GDPR), Clinical Trials and Local Legislation
03-10-16 June 2020
Online

ONLINE TRAINING: General Data Protection Regulation (GDPR), Clinical Trials and Local Legislation

A training for understanding the impact of GDPR in clinical trials both at local and international level

WEBINAR: From Theory to Practice: Data Integrity
09, 11, 16 e 18 June - starting time 2.30 pm CEST
Webinar

WEBINAR: From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

ONLINE TRAINING: FDA Medical Devices Registration
11-16-18 June 2020
Online

ONLINE TRAINING: FDA Medical Devices Registration

Different submission types and how to prepare a 510K

ONLINE TRAINING: Writing a Clinical Trial Protocol
09-16-23 June 2020
Online

ONLINE TRAINING: Writing a Clinical Trial Protocol

Which information goes in a protocol. How should we write this information and who is involved

ONLINE TRAINING Medical Writing: Improve your Writing & Reviewing Skills
17-19-24 June 2020
Online

ONLINE TRAINING Medical Writing: Improve your Writing & Reviewing Skills

Writing, editing & proofreading tips for medical writers: a standardised process to make your message effective, review & ensure document quality

ONLINE TRAINING: Market Access: Ways and Methods of Measuring the Value of a Drug or a Medical Device
9-11-17-22-25 June 2020
Online training

ONLINE TRAINING: Market Access: Ways and Methods of Measuring the Value of a Drug or a Medical Device

How payers measure the value of a given product

ONLINE TRAINING: Audit Trail Review
23 - 30 June 2020
Online

ONLINE TRAINING: Audit Trail Review

From regulations to practice

ONLINE TRAINING: Patient Support Program (PSP)
18-23-26-30 June 2020
Online

ONLINE TRAINING: Patient Support Program (PSP)

Strategies, limitations and experiences of a PSP

ONLINE TRAINING: Device Drug and Drug Device Combination Products in the EU under the Medical Devices Regulation (MDR)
25 - 26 - 30 June 2020
Online

ONLINE TRAINING: Device Drug and Drug Device Combination Products in the EU under the Medical Devices Regulation (MDR)

A targeted training to understand the regulatory pathway of device drug and drug device combinations (DDCP) in the European Union
Latest updates from the MDR 2017/745 and EMA guidance

ONLINE TRAINING: How to write a Clinical Evaluation Report from MDR Perspective
25-29 June, 1 July 2020
Online

ONLINE TRAINING: How to write a Clinical Evaluation Report from MDR Perspective


ONLINE TRAINING: La gestione del Case Processing in Farmacovigilanza
02 and 07 July 2020
Online

ONLINE TRAINING: La gestione del Case Processing in Farmacovigilanza

Raccolta, gestione e trasmissione delle segnalazioni di sospette reazioni avverse

ONLINE TRAINING: Medical Reading of Scientific Articles
08 and 10 July 2020
Online

ONLINE TRAINING: Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

ONLINE TRAINING: The Use of EudraVigilance Data Analysis System (EVDAS) in the Signal Management System
08 and 10 July 2020
Online

ONLINE TRAINING: The Use of EudraVigilance Data Analysis System (EVDAS) in the Signal Management System

Close Menu
×
×

Cart

Terms & Conditions

Trainings
The fee includes: tuition, teaching materials, lunches and coffee breaks, organizational office assistance, attendance certificate. Early Bird discount not applicable to Freelance – Academy – Public Administration fee.
The course will proceed with a minimum of 8 participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.
For further information please contact:  e-mail: training@LSAcademy.com  telephone: +39 (0)35.515684

Conferences
The fee includes: seat at the conference, copy of presentations of Speakers who allow the distribution, informative literature for the day, networking lunch, coffee break, organisational office assistance, certificate of attendance. For further information please contact:  e-mail: events@LSAcademy.com  telephone: +39 (0)35.515684

Webinars
The fee includes: tuition, teaching materials, organizational office assistance, attendance certificate. Early Bird discount not applicable to Freelance – Academy – Public Administration fee. For further information please contact:  e-mail: training@LSAcademy.com  telephone: +39 (0)35.515684

Common Terms & Conditions

Terms of payment
Payment should be made online (by credit card) or by bank transfer, at the time of registration (only for Italian companies: + 22% VAT) to EasyB s.r.l by bank transfer or by credit card. Bank transfer payable to:

EasyB S.r.l.
Via Roma, 20 – 24022 Alzano Lombardo (Bergamo)
VAT: IT03633040161
BANCO BPM – Filiale di Carobbio degli Angeli
IBAN: IT81 F 05034 53960 000000003450
SWIFT Code: BAPPIT21AY5

Confirmation of event admission will be given on receipt of payment. Invoice will be sent following receipt of payment. EasyB reserves the right to refuse late registrations or additional registrations above the maximum accepted number of participants or registrations of roles that are not included in the target of the event.

Cancellation
Please note that refunds (50% refund of the registration fee) will only be given if cancellation is received at least four weeks before the event date. Cancellations will only be valid if made in writing. Transfer of registrations (or name changes) are allowed for free and should be made in writing within 7 days prior to the event. EasyB reserves the right to postpone or cancel an event, to change the location of an event or to alter the advertised speakers for an event, to change its performance from residential to webinar/online. EasyB is not responsible for any loss or damage as a result of substitution, alteration, postponement or cancellation of an event due to causes beyond its control including without limitation, acts of God, natural disasters, sabotage, accident, trade of industrial disputes, terrorism, hostilities, epidemics, pandemics, and / or authorities’restrictions (so-called factum principis).

Information collection and use
In accordance with the Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016, we inform you that EasyB S.r.l. (with headquarter in Via Roma 20, Alzano Lombardo, Bergamo, Italy, VAT number IT03633040161) will use your personal data voluntarily provided by you only with the consent and in compliance with the principles dictated by the European Regulations on the protection of personal data for sending newsletters, for marketing purposes (sending advertising material, market research and commercial communication) and for communication purposes to third parties (lecturers, scientific board, speakers, conferences’ sponsor), also for marketing goals. You can read the complete information, including your rights and the procedures for the exercise of the same, following this link.