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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

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

Biomedical Literature, Databases and Bibliometric Indicators

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

10 March 2020

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

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

From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

24 March 2020

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

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

Data Transparency: Its Impact on Clinical Trials

Effectively facing with the new environment of clinical studies

21-22 April 2020

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

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

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

13 - 14 May 2020

Quality, Compliance
and Audit in GVP

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

13 May 2020

Quality Risk Management – Workshop

A definition of the risk management process in clinical research

26-27 May 2020

Clinical Evaluation and Investigation of Medical Devices

A new approach following the European Regulation MDR 2017/745

26 May 2020

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

Searching the Medical Literature

How and where to find the biomedical data you need

04 June 2020

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

Writing Articles for Peer-Reviewed Journals in the Health Sciences

How to write a scientific paper

29 - 30 September 2020

From Theory to Practice: Data Integrity

Implementing GxP Data Integrity regulations on everyday practice

20 - 21 October 2020

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

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

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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:  telephone: +39 (0)35.515684

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:  telephone: +39 (0)35.515684

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