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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

Clinical Research

Courses on Clinical Research address Clinical Research on humans and guide participants on the methodological, logistical and documentation needs. Courses on Clinical Research (interactive workshops seminars, discussion) may be of interest to those who work in the life cycle of a pharma product or of a medical device.

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Courses found: 31
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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

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

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


Webinar
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
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


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 Risk Management – Workshop
13 May 2020
Milan

Quality Risk Management – Workshop

A definition of the risk management process in clinical research

Real-World Data and Real-World Evidence
12 - 13 May 2020
Milan

Real-World Data and Real-World Evidence

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

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

Webinar
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

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

Clinical Evaluation and Investigation of Medical Devices
26-27 May 2020
Milan

Clinical Evaluation and Investigation of Medical Devices

A new approach following the European Regulation MDR 2017/745

Searching the Medical Literature
4 June 2020
Budapest

Searching the Medical Literature

How and where to find the biomedical data you need

Writing Articles for Peer-Reviewed Journals in the Health Sciences
04-05 June 2020
Barcelona

Writing Articles for Peer-Reviewed Journals in the Health Sciences

How to write a scientific paper

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

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

WEBINAR: 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

Writing a Clinical Trial Protocol
22 June 2020
Milan

Writing a Clinical Trial Protocol

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

Audits and Auditors 4.0 Working According to GxP
24-25 June 2020
Milan

Audits and Auditors 4.0 Working According to GxP

Innovative Approaches to Audit and Challenges for Auditors Working on New Requirements and Emerging Technologies

The Medical Device Clinical Evaluation
07 July 2020
Copenhagen

The Medical Device Clinical Evaluation

Understanding the clinical evaluation requirements for the MedTech industry
Latest news from MDR 2017/745 and ISO 14155!

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 

Medical Reading of Scientific Articles
08-09 July 2020
Milan

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

Data Transparency: Its Impact on Clinical Trials
14 - 15 September 2020
Berlin

Data Transparency: Its Impact on Clinical Trials

Effectively facing with the new environment of clinical studies

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 Reading of Scientific Articles
22 - 23 October 2020
Barcelona

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

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

Comparison with problems faced in other working realities

Usefulness of the information acquired

Number of people contained wich allows interaction

It is not a frontal lesson but an interactive one

Practical examples carried out during the lessons

Practical evaluation of how to approach risk analysis

The teacher is very competent

Detailed analysis of operating methods

The venue is very beautiful and LS Academy staff was efficient

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