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for Pharmaceutical and Medical Devices Professionals

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Clinical Research Centers

Clinical Research Centers

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Courses found: 21
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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

4 March 2020
Milan

Biomedical Literature, Databases and Bibliometric Indicators

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

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

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

24 - 25 March 2020
Milan

From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

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

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

20 - 21 April 2020
Berlin

Data Transparency: Its Impact on Clinical Trials

Effectively facing with the new environment of clinical studies

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 

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!

29 - 30 April 2020
Milan

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

13 - 14 May 2020
Milan

Quality, Compliance
and Audit in GVP

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

13 May 2020
Milan

Quality Risk Management – Workshop

A definition of the risk management process in clinical research

26-27 May 2020
Milan

Clinical Evaluation and Investigation of Medical Devices

A new approach following the European Regulation MDR 2017/745

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

4 June 2020
Budapest

Searching the Medical Literature

How and where to find the biomedical data you need

04 June 2020
Budapest

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

04-05 June 2020
Barcelona

Writing Articles for Peer-Reviewed Journals in the Health Sciences

How to write a scientific paper

29 - 30 September 2020
Madrid

From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

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

22 - 23 October 2020
Barcelona

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

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