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for Pharmaceutical and Medical Devices Professionals

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Medical Writing

Medical Writing or the drafting, reviewing and editing of medical texts includes both regulatory writing and medical communications. In these courses, participants increase their practical skills in writing a medical text, the structure it needs to have and how to appropriately review it. The courses on Medical Writing are designed for those who need to prepare documentation related to medicines or medical devices: from clinical research protocols, to manuscripts or regulatory submissions. Through our Medical Writing trainings, you may learn the skills needed to convey your key message to your reader with the appropriate form and format.

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Courses found: 10
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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: 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

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

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


Webinar
WEBINAR: Writing a Clinical Trial Protocol
09-16-23 June 2020
Webinar

WEBINAR: Writing a Clinical Trial Protocol

Which information goes in a protocol. How should we write this information and who is involved

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 

Data Transparency: Its Impact on Clinical Trials
14 - 15 September 2020
Berlin

Data Transparency: Its Impact on Clinical Trials

Effectively facing with the new environment of clinical studies

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 

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

Participants' Feedbacks

Very good switches, shifts between listening and doing exercises

Now have more structured approach to writing on article

Very practical and constructive - readily helpful

broader view on publication writing

Environment was well described. I appreciated a lot the number of exercises

Practical and clear explanations

very effective training with exercises

Perfect time for discussions, and sharing of experiences

Very focused and pragmatic

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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
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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).

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