The life cycle of a medicine, from its design to its marketing, including its manufacturing and distribution, is a complex and rigorously regulated process. Each step of this journey is essential to ensure the safety and effectiveness of treatments administered to patients.

The different phases of the medication management cycle

The medication management cycle can be divided into several key phases:

Research and development

This phase begins with the identification of a new molecule or a new active substance, followed by a series of laboratory tests and on animal models to evaluate its therapeutic potential and its toxicity.

Production

Once clinical trials are successful, the drug is produced on a large scale in pharmaceutical factories, following strict quality standards.

Marketing

After obtaining marketing authorizations, the drug is distributed to pharmacies and hospitals.

Post-market surveillance

Even after marketing, the drug continues to be monitored for possible long-term adverse effects and to assess its effectiveness in larger populations.

The importance of safety and effectiveness
The safety and effectiveness of a medicine are two essential criteria to guarantee the protection of public health. To achieve this balance, health authorities put in place strict regulations and rigorous control procedures throughout the life cycle of the medicine.

The safety of a medicine is ensured by:

The effectiveness of a drug is demonstrated by :

The challenges of medication management

Medication management is a major public health issue. It involves many stakeholders, such as pharmaceutical laboratories, health authorities, health professionals and patients. The main challenges of this management are:

The medicines management cycle is a complex process that requires close coordination between all stakeholders involved. By ensuring the safety and effectiveness of medicines, we help improve public health and extend life expectancy.