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for Pharmaceutical and Medical Devices Professionals

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  • Evaluation of expectations achievement

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Clinical Research

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Courses found: 18
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New EU Medical Devices Regulation 2017/745 Training Course: Get Ready to Implement the MDR!
19 - 20 February 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

Biomedical Literature, Databases and Bibliometric Indicators
4 March 2020
Milan

Biomedical Literature, Databases and Bibliometric Indicators

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

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

EudraVigilance, EVDAS and MLM service
11 - 12 March 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

Device Drug and Drug Device Combination Products in the EU under the Medical Devices Regulation (MDR)
17 March 2020
Vienna

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

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

Writing a Clinical Trial Protocol
24 March 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
07-08 April 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

Data Transparency: Its Impact on Clinical Trials
20 - 21 April 2020
Berlin

Data Transparency: Its Impact on Clinical Trials

Effectively facing with the new environment of clinical studies

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 

The Medical Device Clinical Evaluation
22 April 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!

Medical Reading of Scientific Articles
29 - 30 April 2020
Milan

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

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

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

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

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

Participants' Feedbacks

Detailed analysis of operating methods

Usefulness of the information acquired

Number of people contained wich allows interaction

Comparison with problems faced in other working realities

Practical evaluation of how to approach risk analysis

The teacher is very competent

Practical examples carried out during the lessons

It is not a frontal lesson but an interactive one

The venue is very beautiful and LS Academy staff was efficient

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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

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