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

Regulatory

How to best comply with local, European and international regulations in the healthcare field. The courses on Regulatory Affairs offer a practical overview on regulations in place: from the local submission of a new study to the European regulations and requirements. These Regulatory trainings are designed for those who need updated and strong regulatory knowledge for their routine activities.

Refine search


Courses found: 17
Order by
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

Webinar
Webinar: Biomedical Literature, Databases and Bibliometric Indicators
13-19-21 May 2020
Webinar

Webinar: Biomedical Literature, Databases and Bibliometric Indicators

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

Webinar
WEBINAR – Promotion of a Pharmaceutical Brand
21 May, 28 May, 04 June 2020, h. 10:30 am
Webinar

WEBINAR – Promotion of a Pharmaceutical Brand

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

Patient Support Program (PSP)
21-22 May 2020
Milan

Patient Support Program (PSP)

Strategies, limitations and experiences of a PSP

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

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

Webinar
Webinar: Medical Devices Registration at an International Level
3 - 4 - 10 June 2020
Webinar

Webinar: 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

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 

Webinar
Webinar: Device Drug and Drug Device Combination Products in the EU under the Medical Devices Regulation (MDR)
25 - 26 - 30 June 2020
Webinar

Webinar: 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

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product: From Patients to Health Authorities
07-08 July 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
08-09 July 2020
Milan

Medical Reading of Scientific Articles

The critical evaluation of the scientific paper

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

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product: From Patients to Health Authorities
13-14 Oct 2020
Copenhagen

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 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

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

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!

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

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)

Excellent interaction between teachers and participants

Close Menu
×
×

Cart

Terms & Conditions

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

Webinars
The fee includes: tuition, teaching materials, organizational office assistance, attendance certificate. Early Bird discount not applicable to Freelance – Academy – Public Administration fee. For further information please contact:  e-mail: training@LSAcademy.com  telephone: +39 (0)35.515684

Common Terms & Conditions

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:

EasyB S.r.l.
Via Roma, 20 – 24022 Alzano Lombardo (Bergamo)
VAT: IT03633040161
BANCO BPM – Filiale di Carobbio degli Angeli
IBAN: IT81 F 05034 53960 000000003450
SWIFT Code: BAPPIT21AY5

Confirmation of event admission will be given on receipt of payment. Invoice will be sent following receipt of payment. EasyB reserves the right to refuse late registrations or additional registrations above the maximum accepted number of participants or registrations of roles that are not included in the target of the event.

Cancellation
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, to change its performance from residential to webinar/online. 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, hostilities, epidemics, pandemics, and / or authorities’restrictions (so-called factum principis).

Information collection and use
In accordance with the Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016, we inform you that EasyB S.r.l. (with headquarter in Via Roma 20, Alzano Lombardo, Bergamo, Italy, VAT number IT03633040161) will use your personal data voluntarily provided by you only with the consent and in compliance with the principles dictated by the European Regulations on the protection of personal data for sending newsletters, for marketing purposes (sending advertising material, market research and commercial communication) and for communication purposes to third parties (lecturers, scientific board, speakers, conferences’ sponsor), also for marketing goals. You can read the complete information, including your rights and the procedures for the exercise of the same, following this link.