Discover all the

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

Medical Device

These trainings address the different topics related to Medical Devices, either low risk, high risk or in vitro diagnostic Devices. From different local regulations, to European and International markets. These courses are designed for professionals involved in the life cycle of the different Medical devices and who wish to increase their knowledge or who, instead, face the world of Medical Devices for the first time. Courses are held as interactive workshops, with lectures, discussions, and exercises.

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Courses found: 21
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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

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

Labelling Requirements for Medical Devices under the Medical Devices Regulation 2017/745 (MDR)
02 April 2020
Vienna

Labelling Requirements for Medical Devices under the Medical Devices Regulation 2017/745 (MDR)

A one-day training to understand medical device Labelling requirements under the MDR 2017/745

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

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

FDA Medical Devices Registration
29 April 2020
Milan

FDA Medical Devices Registration

Different submission types and how to prepare a 510K

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

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

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

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

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

How to write a Clinical Evaluation Report from MDR Perspective
08 June 2020
Amsterdam

How to write a Clinical Evaluation Report from MDR Perspective


Planning and Running a Hospital Meeting
16-17 June 2020
Milan

Planning and Running a Hospital Meeting

A training course that analyses the key elements of a successful Hospital Meeting

Implementation of the 2017/745 MDR by Notified Bodies: Weaknesses of the Technical Documentation
25 June 2020
Milan

Implementation of the 2017/745 MDR by Notified Bodies: Weaknesses of the Technical Documentation

Insights of the MDR and most relevant issues identified by Notified Bodies during the evaluation process 

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

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

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

Variety of topics covered, which have been adapted to the different needs of the participants

International and multidisciplinary profile of participants, which enriches the training

Availability and competence of the lecturer

The limited number of participants allows a better interaction with the teachers, who can answer all the questions

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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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Terms of payment
Payment should be made online (by credit card) or by bank transfer, at the time of registration (only for Italian companies: + 22% VAT) to EasyB s.r.l by bank transfer or by credit card. Bank transfer payable to:

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Please note that refunds (70% refund of the registration fee) will only be given if cancellation is received at least one week before the event date. Cancellations will only be valid if made in writing. Transfer of registrations (or name changes) are allowed and should be made in writing within 7 days prior to the event. EasyB reserves the right to postpone or cancel an event, to change the location of an event or to alter the advertised speakers for an event. EasyB is not responsible for any loss or damage as a result of substitution, alteration, postponement or cancellation of an event due to causes beyond its control including without limitation, acts of God, natural disasters, sabotage, accident, trade of industrial disputes, terrorism, or hostilities.

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