Drug Life Cycle E-learning (asynchrone)
Dernière mise à jour : 25/06/2026
Description
A drug follows a complex path, strictly regulated by health authorities, from its discovery through to its marketing and, where applicable, its transition to a generic drug.
Through a 10-minute educational video, this module provides an overview of the main stages of a drug's lifecycle and the regulatory requirements that govern its development, manufacturing, approval, and post-marketing surveillance.
This training serves as an excellent introduction to understanding the pharmaceutical regulatory environment and the stakeholders involved throughout a drug's lifecycle.
Through a 10-minute educational video, this module provides an overview of the main stages of a drug's lifecycle and the regulatory requirements that govern its development, manufacturing, approval, and post-marketing surveillance.
This training serves as an excellent introduction to understanding the pharmaceutical regulatory environment and the stakeholders involved throughout a drug's lifecycle.
Domaine : MEDICAMENTS
Objectifs de la formation
By the end of this module, participants will be able to:
- Identify the key stages of the drug lifecycle, from discovery to market launch.
- Understand the main regulations applicable to each stage of development.
- Recognize the various stakeholders involved in the drug development process.
- Understand the quality, safety, and regulatory compliance issues associated with the pharmaceutical sector.
Public visé
This training is designed for anyone interested in learning about or gaining a better understanding of the pharmaceutical industry and the drug lifecycle, whether they are new to the sector or involved in activities related to medications.
Prérequis
No prerequisites
Programme
Topics covered:
- Drug discovery and development
- Preclinical and clinical studies
- Marketing authorization (MA)
- Manufacturing and distribution
- Pharmacovigilance and post-marketing surveillance
- Generic drugs and end-of-life
- Key regulations applicable throughout the drug development process
Modalités pédagogiques
Interactive module in video format.
Moyens et supports pédagogiques
Once your purchase is complete, you will first receive an order confirmation email.
Then, within 48 hours (business days, after payment is received), you will receive an email confirming your access to the module on our TREENING platform. This access is personal and password-protected.
Tree Support is available to assist you with any technical or functional questions.
For questions specific to the module's subject matter, you can contact us via the discussion forum. One of our experts will respond as soon as possible.
Upon completion of your training, you will be invited to complete a satisfaction survey and, if applicable, download a training certificate.
Then, within 48 hours (business days, after payment is received), you will receive an email confirming your access to the module on our TREENING platform. This access is personal and password-protected.
Tree Support is available to assist you with any technical or functional questions.
For questions specific to the module's subject matter, you can contact us via the discussion forum. One of our experts will respond as soon as possible.
Upon completion of your training, you will be invited to complete a satisfaction survey and, if applicable, download a training certificate.
Modalités d'évaluation et de suivi
- Multiple-choice assessment
- Training certificate: yes
Infos complémentaires
- Module validity: 1 week after payment is received (extension available)
- For orders of more than 10 accesses, contact the training department for a customized quote: [email protected]
- For orders of more than 10 accesses, contact the training department for a customized quote: [email protected]