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 Affairs

Medical Affairs comprises clinical research, development, disease awareness, communications and liaison roles, scientific publications and medical evaluations; all shaping the world of pharma and medical devices of today. Medical Affairs courses address this ever-changing field and are designed for professionals responsible of managing drugs/devices within the field. Through our Medical Affairs workshops, seminars and hands-on sessions one may increase the knowledge and expertise needed on the different regulations and documents (protocols, manuscripts, reports, etc.), as well as on the implementation and conduct of clinical trials.

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Courses found: 21
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Webinar
WEBINAR: Natural Language Processing (NLP) and Text Mining: a Help in Daily Pharmacovigilance Activities
15 April 2020 at 11.00 am
Webinar

WEBINAR: Natural Language Processing (NLP) and Text Mining: a Help in Daily Pharmacovigilance Activities

How to exploit “machine aided” technologies to increase the effectiveness of Pharmacovigilance procedures

Webinar
WEBINAR: Gli Strumenti Statistici per Pianificare e Comprendere Uno Studio Clinico
22-29 April, 06 May 2020
Webinar

WEBINAR: Gli Strumenti Statistici per Pianificare e Comprendere Uno Studio Clinico


Real-World Data and Real-World Evidence
12 - 13 May 2020
Milan

Real-World Data and Real-World Evidence

An intensive Lab Workshop to learn the main concepts behind Real-World Evidence and Observational Research and to design innovative studies that generate evidence

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

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

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

Webinar
WEBINAR: The Strategic Role of the Medical Science Liaison during a Product’s Life Cycle
18-19-27 May, 10 June 2020
Webinar

WEBINAR: The Strategic Role of the Medical Science Liaison during a Product’s Life Cycle

Four modules training to learn and experience the role of a MSL

Designing and Running a Scientific Symposium
11-12 June 2020
Milan

Designing and Running a Scientific Symposium

A comprehensive project-management approach to deliver an effective symposium

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

Workshop: Senior MSL and MSL Manager – the Evolution of a Complex Role
23 June 2020
Milan

Workshop: Senior MSL and MSL Manager – the Evolution of a Complex Role

Experiences on the governance of a Medical Science Liaison (MSL) team

Webinar
Webinar: Market Access: Ways and Methods of Measuring the Value of a Drug or a Medical Device
9-11-17-22-25 June 2020
Webinar

Webinar: Market Access: Ways and Methods of Measuring the Value of a Drug or a Medical Device

How payers measure the value of a given product

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

Medical Writing: from theory to practice
16 - 17 November 2020
Milan

Medical Writing: from theory to practice

Deepening in the environment of scientific publications to write scientific articles achieving the desired objectives

Designing and Running a Scientific Symposium
26-27 November 2020
Budapest

Designing and Running a Scientific Symposium

A comprehensive project-management approach to deliver an effective symposium

Participants' Feedbacks

The small group made it possible to interact very much with the teachers and to create an atmosphere of feeling and trust that allowed us to ask all possible questions

Thank you very much for your wide training offer and for your professionalism. I hope to have the opportunity to attend other courses with you.

Excellent points to share and ideas in daily practice to make your own

Practical exercises have been extremely useful

Very appreciated exercises and role playing

Answers to all questions!

Interactive, practical course that has inspired questions and curiosities

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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

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

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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:

EasyB S.r.l.
Via Roma, 20 – 24022 Alzano Lombardo (Bergamo)
VAT: IT03633040161
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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).

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