Educational and Career Pathways
in Life Sciences

LS Academy organises technical and scientific conferences and training events for professionals in the pharma, medical devices, and related areas working for the industry, CROs, clinical research, and health-related fields.

Training

Onsite // Online // Webinar

Topics covered: Clinical Research, IVDs (In-Vitro Diagnostics), Market Access, Medical Affairs, Medical Device, Medical Writing, Pharmacovigilance, Real World Data and Real World Evidence, Regulatory, Soft Skill, Statistics and Data Management.

05 March 2021
Pharmacovigilance

“Attributability” in Pharmacovigilance: Still a Hot Topic

English
08, 10 and 12 March 2021
Medical Writing

Medical Writing Course: Improve your Writing & Reviewing Skills

English
11 marzo 2021
Medical Affairs / Soft Skill

Webinar: La Gestione dell’Advisory Board nei Progetti Life Science

Italiano
From 15 March to 28 October 2021
Medical Writing

Medical Writing Paths: 'Medical Communications' & 'Regulatory Writing'

English
All courses

Conferences

Face-to-face // Virtual

Since 2010 LS Academy organises local, and international conferences in several European countries.
The topics covered include: clinical research, pharmacovigilance and surveillance, statistics, directives and regulations, data transparency, and epidemiology.

04, 05 e 06 maggio 2021
Clinical Research

Italian ePharma Day

Italiano
14 - 18 June 2021
Pharmacovigilance

International Pharmacovigilance Days

English
21 - 24 September 2021
Medical Device

MedDev Day

English
28 September 2021
Clinical Research

Patient Partnering in Clinical Development

English
All conferences Become Sponsor

LS Academy by numbers

2010
Foundation Year
483
Training run
96
Conferences held
9000
Professionals trained

Some of our services

In-house Training
In-house Training
Customized solutions for in-company training
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Investigators’ Meeting
Investigators’ Meeting
Preparation and organisation of Investigators’ Meeting
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Medical Writing
Medical Writing
Specialized support for planning and management of scientific documentation
View more
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Testimonials

Congratulations for the great organisation of the event and the high level of the speakers. I really enjoyed the meeting!
Medical Director - Sanofi
It was a good balance of lectures, examples and some role play. Enough time for questions as well.
Director, Clinical Operations - Chiesi Farmaceutici
Excellent points to share and ideas in daily practice to make your own
Farmacovigilance Manager - Celgene
Thank you very much for your wide training offer and for your professionalism. I hope to have the opportunity to attend other trainings with you.
Medical Science Liaison - FullCro
Congratulations for the great organisation of the event and the high level of the speakers. I really enjoyed the meeting!
Medical Director - Laboratorios Farmacéuticos Rovi
The small group allowed us to interact a lot with the teacher and to create a climate of feeling and trust that allowed us to ask all possible questions
Clinical Affairs Specialist - Kyowa Kirin
Only positive feedback: very expert presenters in this field, very good discussion at high level
Clinical R&D Manager - Boston Scientific
Discussion of the topics covered not only from a Pharmacovigilance point of view, but considering the interactions with other company functions / departments
Senior Advisor of R&D - Kedrion
Interaction with different player involved in clinical trials. Sharing info into different companies/organization
Scientific Affairs Manager - italfarmaco
The theory parts were supported by very good concrete examples, which was great. Trainer was good and allowed for questions.
Director, Clinical Operations - OPIS
Good agenda very informative. Speakers and participants from different backgrounds and broad coverage of the topic
Senior Legal Counseil - Novo Nordisk
Thank you very much for all organizing efforts and for an excellent conference
Medical Advisor - Mylan Italia
Interactive, practical course that inspired questions and curiosities. Continue concrete and real examples for the best understanding
Quality Assurance and Clinical Affairs Associate - Ferring
Group size very useful for intense discussion and communications
Clinical Study Coordinator - LEO Pharma
Variety of topics, key messages around clinical impact were detailed well, speakers engaging and knowledgeable
Regulatory Manager - Alk Abellò
International and multidisciplinary profile of participants, which enriches the training
Clinical Operations Manager - Asphalion