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Courses

for Pharmaceutical and Medical Devices Professionals

  • Selected highly recognised teachers
  • Personalised needs Analysis
  • Updated programs and topics
  • A limited number of participants
  • Evaluation of expectations achievement

Pharmacovigilance

Pharmacovigilance courses deal with the latest news on the evaluation and prevention of adverse events or other medical related events, to ensure a good benefit/risk profile for patients: regulations in place, strategy, methodology and even the use of artificial intelligence in the field of pharmacovigilance. These trainings are designed for clinical research professionals who wish to know more about Pharmacovigilance or for those already in the field who need a high-level training. Courses on Pharmacovigilance are held as interactive workshops, with lectures, discussions and exercises.

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Courses found: 14
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Webinar
WEBINAR: Beyond PubMed
7 April 2020 at 2.00 pm
Webinar

WEBINAR: Beyond PubMed

Additional approaches and sources for cost-effective literature monitoring

Webinar
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
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

Quality, Compliance and Audit in GVP
13 - 14 May 2020
Milan

Quality, Compliance
and Audit in GVP

How to apply Good Pharmacovigilance Practices (GVPs) to Quality Management and Pharmacovigilance Auditing

Medical Writing: Improve your Writing & Reviewing Skills
26 May 2020
Copenhagen

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

From Theory to Practice: Data Integrity
09-10 June 2020
Milan

From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

EudraVigilance, EVDAS and MLM service
15 - 16 June 2020
Milan

EudraVigilance, EVDAS and MLM service

Training on the EudraVigilance system focusing on EVDAS (EudraVigilance Data Analysis System) and MLM (Medical Literature Monitoring): critical aspects, challenges, and opportunities

Artificial Intelligence in Pharmacovigilance and New Technologies. Do We Really Need them?
24 - 25 June 2020
Budapest

Artificial Intelligence in Pharmacovigilance and New Technologies. Do We Really Need them?

An overview of what the new digital technologies can do to improve cost/effectiveness and quality of Pharmacovigilance activities

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product: From Patients to Health Authorities
07-08 July 2020
Rome

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product: From Patients to Health Authorities

Development Safety Update Report (DSUR), Risk Management Plan (RMP), Periodic Safety Update Report (PSUR) / Periodic Benefit-Risk Evaluation Report (PBRER), and Addendum to the Clinical Overview 

From Theory to Practice: Data Integrity
29 - 30 September 2020
Madrid

From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

Pharmacovigilance Oversight
29 September 2020
Amsterdam

Pharmacovigilance Oversight

How to guarantee quality and to manage pharmacovigilance audits and inspections succesfully in PV oversight activities

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product: From Patients to Health Authorities
13-14 Oct 2020
Copenhagen

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product: From Patients to Health Authorities

Development Safety Update Report (DSUR), Risk Management Plan (RMP), Periodic Safety Update Report (PSUR) / Periodic Benefit-Risk Evaluation Report (PBRER), and Addendum to the Clinical Overview 

The EU Medical Devices Regulation 2017/745
20 - 21 October 2020
Vienna

The EU Medical Devices Regulation 2017/745

Understanding the Medical Devices Regulation and its impact on Industry
Latest updates after the MDR 2017/745 date of application

Medical Writing: from theory to practice
16 - 17 November 2020
Milan

Medical Writing: from theory to practice

Deepening in the environment of scientific publications to write scientific articles achieving the desired objectives

Participants' Feedbacks

Teachers very expert and very good in comunication

Exhaustive, interactive and clear explanations

Discussion of the topics covered by the course, not only from the Pharmacovigilance point of view, but considering the interactions with other functions / other company departments

I was put at ease during the course and the discussions

Teacher very expert on the subject, available  with the participants, exhaustive in the explanations

Choice of topics of great importance for pharmacovigilance activities

LS Academy secretariat available to facilitate enrollment of more than one person from the same company

Speakers very capable in deepening vast and complex topics

The course gave me clear examples

Teacher was very clear  and outstanding  knowledge of the contents 

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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
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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 (70% refund of the registration fee) will only be given if cancellation is received at least one week before the event date. Cancellations will only be valid if made in writing. Transfer of registrations (or name changes) are allowed 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).

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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.