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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

Regulatory

Regulatory

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Courses found: 17
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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

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

Promotion of a Pharmaceutical Brand
8 April 2020
Milan

Promotion of a Pharmaceutical Brand

Implementing new and traditional pharma promotion channels in accordance to regulations in place

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 

Medical Reading of Scientific Articles
29 - 30 April 2020
Milan

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

FDA Medical Devices Registration
29 April 2020
Milan

FDA Medical Devices Registration

Different submission types and how to prepare a 510K

Advanced European Regulatory Affairs
07 - 08 May 2020
Amsterdam

Advanced European Regulatory Affairs

Update on Regulatory Affairs developments in Europe and the impact on product development and life cycle management

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

Medical Devices Registration at an International Level
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

Audit Trail Review – Workshop
16 June 2020
Milan

Audit Trail Review – Workshop

From regulations to practice

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

Audit Trail Review – Workshop
3 November 2020
Copenhagen

Audit Trail Review – Workshop

From regulations to practice

Participants' Feedbacks

Topics which are not included in other educations I've been on (orphans, ATMP and similar)

International and multidisciplinary profile of participants, which enriches the training

no standard workshop which is very stressful so the way that this course was conducted was excellent and the first one for me were I was so relaxed… thank you for that feeling!

Lecturers know what they are talking about and are able to answer the questions. It's clear that they work and have experience in the field

Excellent interaction between teachers and participants

Exemples from real life situations from the workplace were very useful.

Good atmosphere in the group and interaction with the lecturers (really available for all questions)

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