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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.
Medical Writing
Have you ever wondered what distinguishes average writing assistance
from an excellent medical writing service?
CONTACT US
Conferences 2024
GERMAN PHV DAY - 17 September 2024 | Frankfurt am Main
MEDDEV DAY - 07 and 08 October 2024 | Copenhagen
ITALIAN PHV DAY - 23 October 2024 | Bergamo
NORDIC PHV DAY - 13 November 2024 | Copenhagen
DISCOVER MORE

Training

Onsite // Online // Webinar

To enhance and add value to your skills while staying up-to-date

20 and 21 February 2025
Medical Device

Labelling Requirements for Medical Devices

English
NEW
24 and 26 February 2025
Animal Health / Pharmacovigilance

Reporting Requirements in Veterinary Pharmacovigilance

English
NEW
13 and 14 March 2025
Medical Device / Medical Writing

Mastering MDCG 2024-3: Comprehensive Training on Clinical Investigation Plans

English
18, 20 e 25 marzo 2025
Medical Device / Medical Affairs / Medical Writing / Clinical Research

La Statistica Medica per Non Statistici

Italiano
Tutti i corsi

Training Paths

Highly specialised training courses to give you a technical and practical background to excel in the specialised field of Life Sciences

Tutti i percorsi formativi

Conferences

Opportunities of training and professional growth, to build and consolidate your network

27 October 2025
Statistics and Data Management

European Statistical Forum

English
Tutte le conferenze Become Sponsor

LS Academy by numbers

2010
Foundation Year
773
Training run
115
Conferences held
12177
Professionals trained
410
Lecturers and Speakers
264
Delivered Medical Writing services

Some of our services

In-house Training
In-house Training
Customized solutions for in-company training
View more
Investigator Meetings
Investigator Meetings
Preparation and organisation of Investigator Meetings
View more
Medical Writing
Medical Writing
Unleash the power of words, weaving meanings into scientific texts
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
Pharmacovigilance Manager - Celgene
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
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
PV Manager - 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 - Ferring
Group size very useful for intense discussion and communications
Regulatory Manager - LEO Pharma
Variety of topics, key messages around clinical impact were detailed well, speakers engaging and knowledgeable
Regulatory Manager - Alk Abellò
Varietà di argomenti, i messaggi chiave sull'impatto clinico erano ben dettagliati, i relatori coinvolgenti
Regulatory Manager - Alk Abellò
Il gruppo di lavoro contenuto ha favorito momenti di discussione e la comunicazione efficace
Clinical Study Manager - LEO Pharma
International and multidisciplinary profile of participants, which enriches the training
Regulatory Affairs - Asphalion
Agenda della conferenza molto completa. Relatori e partecipanti di diversa estrazione e ampia copertura dell'argomento
Senior Legal Counseil - Novo Nordisk
Giusto mix tra parti teoriche ed esempi concreti. Trainer preparato e disponibile a rispondere a tutte le domande.
Director, Clinical Operations - OPIS
Interazione con diversi attori coinvolti nelle sperimentazioni cliniche. Condivisione di informazioni da diverse società/organizzazioni
Scientific Manager - Italfarmaco
Discussione degli argomenti oggetto del corso, non solo dal punto di vista della Farmacovigilanza, ma considerando le interazioni con le altre funzioni/altri dipartimenti aziendali
Senior Advisor of R&D - Kedrion
Relatori molto esperti nel campo della farmacovigilanza, ottima discussione ad alto contenuto scientifico
R&D Manager - Boston Scientific
Il gruppo ristretto ha permesso di interagire molto con i docenti e di creare un clima di fiducia, che ci ha permesso di chiarire tutti i dubbi
Clinical Affairs Specialist - Kyowa Kirin
Complimenti per l'ottima organizzazione della conferenza e la competenza degli oratori. Ho apprezzato moltissimo questo meeting!
Medical Director - ISDIN
L'offerta formativa proposta è ampia e variegata. Spero di avere modo di frequentare altri corsi con voi.
Medical Science Liaison - FullCro
Ottimi punti di discussione da condividere e spunti utili nella pratica quotidiana
Pharmacovigilance Manager - Abbott
Buon equilibrio tra lezioni, esempi e alcuni role play. Tempo adeguato anche per le domande.
Director, Clinical Operations - Chiesi Farmaceutici
Ottima organizzazione della conferenza e panel relatori di altissimo livello
Medical Director - GSK

Pharmaceutical training

We understand the critical importance of continuous education in the pharmaceutical sector. Our pharmaceutical training programs are meticulously designed to provide professionals with the knowledge and skills needed to stay at the forefront of the industry. Each course is tailored to meet the specific needs of our participants, ensuring relevance and applicability to their daily responsibilities.

Our courses cover a wide range of topics, from drug development processes and pharmaceutical regulations to quality assurance and market strategies. By participating in our training sessions, professionals gain a deeper understanding of the complexities of the pharmaceutical industry and learn how to navigate its challenges effectively.

Pharma courses

Our pharma courses are structured to provide comprehensive insights into the pharmaceutical industry. Participants can choose from beginner to advanced level courses, each structured to address the learning needs of various professionals in the field. Whether you are a new entrant or an experienced professional, our courses are designed to help you achieve mastery over your area of focus.

From detailed courses on Good Manufacturing Practices and Medical Device to specialized training in clinical trial management and regulatory affairs, LS Academy ensures that all participants receive the education they need to succeed. Our expert trainers are seasoned industry professionals who bring real-world experience into the classroom, making learning practical and applicable.

Medical device training

The medical device sector is rapidly evolving, with innovations and regulatory changes shaping the industry. LS Academy’s medical device training programs are crafted to help professionals understand these dynamics and how to implement them in their work. Our courses cover everything from device design and manufacturing to regulatory compliance and post-market surveillance.

We also emphasize the importance of understanding the European Medical Device Regulation (MDR), which is crucial for professionals working in or with the European market. Our training helps ensure that participants are not only compliant with current regulations but also prepared for future industry shifts.

European medical device regulation

Navigating the complexities of the European Medical Device Regulation (MDR) is essential for any professional involved in the medical device industry in Europe. Our dedicated courses on European medical device regulation delve into the specifics of MDR, its implications for manufacturers, and the necessary steps for compliance.

Participants learn about the regulatory framework, including critical aspects such as risk assessment, clinical evaluation, and the European database on medical devices (EUDAMED). These courses are essential for ensuring that professionals are well-equipped to meet the stringent standards set by European authorities, thus facilitating smoother market entry and enhanced product safety.

Good manufacturing practices

Good Manufacturing Practices (GMP) are the backbone of quality assurance in both the pharmaceutical and medical device industries. At LS Academy, our GMP training is designed to familiarize professionals with the principles and practices necessary to manufacture products that meet both legal and quality standards.

Good manufacturing process

Our training on Good Manufacturing Process extends beyond the basic requirements of GMP to explore advanced concepts necessary for high-level manufacturing operations. This includes detailed analysis of process validation, quality control, and quality assurance measures. Our courses also cover the latest innovations in manufacturing technology and how they can be integrated into existing GMP frameworks to enhance efficiency and reliability.

Life Science

The field of Life Science is broad and encompasses various disciplines that are crucial to the advancement of medical science and healthcare. At LS Academy, our Life Science training programs highlight the interconnectivity of biotechnology, pharmaceuticals, and medical technology. By understanding these relationships, professionals can better contribute to the development of innovative solutions that enhance patient care and treatment outcomes.

Through comprehensive education and training, LS Academy remains committed to advancing the knowledge and skills of professionals in the Life Sciences field, thereby contributing to the overall improvement and innovation within the industry.

LS Academy

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Training

  • Animal Health
  • Clinical Research
  • Evidence Generation
  • GMP (Good Manufacturing Practices)
  • IVDs (In-Vitro Diagnostics)
  • Market Access
  • Medical Affairs
  • Medical Device
  • Medical Writing
  • Pharmacovigilance
  • Regulatory
  • Soft Skill
  • Statistics and Data Management

Conferences

  • Clinical Research
  • Medical Affairs
  • Medical Device
  • Pharmacovigilance
  • Real World Data and Real World Evidence
  • Statistics and Data Management
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