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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: 13
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General Data Protection Regulation (GDPR), Clinical Trials and Local Legislation
10 March 2020
Milan

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

From Theory to Practice: Data Integrity
24 - 25 March 2020
Milan

From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

Artificial Intelligence in Pharmacovigilance and New Technologies. Do We Really Need them?
30 - 31 March 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
21-22 April 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 

Pharmacovigilance Oversight
21 April 2020
Amsterdam

Pharmacovigilance Oversight

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

EudraVigilance, EVDAS and MLM service
28 - 29 April 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

New EU Medical Devices Regulation 2017/745 Training Course: Get Ready to Implement the MDR!
06 - 07 May 2020
Berlin

New EU Medical Devices Regulation 2017/745 Training Course: Get Ready to Implement the MDR!

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

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

Searching the Medical Literature
4 June 2020
Budapest

Searching the Medical Literature

How and where to find the biomedical data you need

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 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

Participants' Feedbacks

Speakers very capable in deepening vast and complex topics

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

Exhaustive, interactive and clear explanations

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

Availability and efficiency of the organization

Teacher was very clear  and outstanding  knowledge of the contents 

The course gave me clear examples

I was put at ease during the course and the discussions

Teachers very expert and very good in comunication

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

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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

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 (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. 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, or hostilities.

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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.