Training Paths

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

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Percorsi Formativi appena svolti

Dal 04 ottobre al 13 dicembre 2024

Medical Affairs

Medical Affairs: Prepararsi alle Sfide Future di un Ruolo Complesso

dal 27 settembre al 23 novembre 2024

Clinical Research

Clinical Quality Assurance: un Ruolo Chiave nella Ricerca Clinica

From 18 September to 23 October 2024

Pharmacovigilance / Medical Writing

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product

Dal 12 marzo al 18 giugno 2024

GMP (Good Manufacturing Practices) / Soft Skill

Percorso Formativo GMP Project Management

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Codice di Buona Condotta

Our highly specialised training courses are the right tool for those who wish to keep up to date within a given area or to deepen their knowledge in a specific subject.

Through our specialised training courses and masterclasses - consisting of a series of courses following the same fil rouge – you have the possibility of getting even more comprehensive training, and gaining a wealth of technical and practical skills to work in a highly-technical life science environment.

Pharmaceutical industry training courses

At LS Academy, we offer an extensive range of pharmaceutical industry training courses designed to elevate the skills and knowledge of professionals at every career level. Our courses cover various aspects of the pharmaceutical industry, ensuring participants are well-equipped to meet industry challenges and excel in their roles.

Quality Assurance courses

Quality Assurance (QA) is a critical component of the pharmaceutical industry, ensuring that products meet the highest standards of safety and efficacy. LS Academy’s Quality Assurance courses are designed to provide professionals with in-depth knowledge and practical skills needed to implement and maintain robust QA systems.

Our courses cover a range of topics, including GMP (Good Manufacturing Practices), quality control, and regulatory compliance. Participants learn about the latest QA methodologies and tools, enabling them to ensure that their company’s products comply with all relevant standards and regulations. These courses also emphasize the importance of continuous improvement and risk management in maintaining product quality.

By participating in our Quality Assurance courses, professionals can enhance their ability to identify and address potential quality issues, implement effective QA processes, and contribute to the overall success of their organization.

Medical affairs training program

The Medical Affairs Training Program at LS Academy is designed to equip professionals with the knowledge and skills necessary to excel in medical affairs roles within the pharmaceutical industry. This program covers essential topics such as medical communication, clinical trial oversight, and regulatory compliance.

Participants in this program will gain a comprehensive understanding of the medical affairs function and its critical role in ensuring the safe and effective use of pharmaceutical products. This training prepares professionals to effectively bridge the gap between clinical development and commercialization.

Regulatory medical devices courses

Regulatory compliance is essential for the successful development and commercialization of medical devices. LS Academy’s Regulatory Medical Devices Courses provide in-depth training on the regulatory requirements and standards applicable to medical devices.

These courses cover a wide range of topics, including the European Medical Device Regulation (MDR), FDA regulations, and other international standards. Participants will learn how to navigate the complex regulatory landscape, prepare and submit regulatory filings, and ensure ongoing compliance throughout the product lifecycle.

Our courses also include practical case studies and real-world examples to help participants understand the application of regulatory requirements in different scenarios. By the end of the course, professionals will be equipped with the knowledge and skills needed to manage regulatory processes effectively and ensure the successful approval and market entry of medical devices.

Training course for MSL: Medical science liaison

The Medical Science Liaison (MSL) role is critical in bridging the gap between pharmaceutical companies and the medical community. LS Academy’s Training Course for MSLs provides comprehensive training to prepare professionals for this essential role.

This course covers key areas such as scientific communication, relationship building with key opinion leaders (KOLs), and the dissemination of clinical and scientific information. Participants will also learn about the strategic importance of the MSL role in supporting product launches, clinical trials, and post-market surveillance.

Through interactive sessions and real-world scenarios, participants will develop the skills needed to excel as MSLs, including effective communication, scientific expertise, and the ability to build and maintain professional relationships. This training ensures that MSLs can effectively support their organizations and contribute to the advancement of medical science.

Pharmacovigilance training

Pharmacovigilance is a vital aspect of the pharmaceutical industry, focused on the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. LS Academy’s Pharmacovigilance Training courses provide professionals with the necessary skills to ensure drug safety and regulatory compliance.

Our courses cover essential pharmacovigilance topics, including adverse event reporting, signal detection, risk management, and regulatory requirements. Participants will learn how to implement and manage effective pharmacovigilance systems, ensuring that their organizations comply with global safety standards.

Through case studies and practical exercises, participants will gain hands-on experience in identifying and managing drug safety issues. This training prepares professionals to proactively address potential risks, improve patient safety, and contribute to the overall success of their organizations.