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Related Concept Videos

Drug Regulation01:25

Drug Regulation

Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
Drug Products: Biologics, Biosimilars and Interchangeables01:28

Drug Products: Biologics, Biosimilars and Interchangeables

Biologics, derived from living sources such as humans, animals, or microorganisms, represent a significant category of pharmaceuticals. These complex molecules, developed through advanced biotechnological methods or purified from natural sources, include essential medical treatments like insulin and growth hormones. The complexity of biologics arises from their large molecular structures and the intricate processes required for their production, making them distinct from conventional...
Prescription, Nonprescription and Orphan Drugs01:02

Prescription, Nonprescription and Orphan Drugs

Prescription drugs require a prescription from a medical practitioner and can only be obtained from a pharmacy. They have many applications, including treating pain, anxiety, and hypertension.
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
Drug Nomenclature01:17

Drug Nomenclature

During the development of a new pharmaceutical, the manufacturer initially assigns a code name to the drug. Once approved, the drug receives a United States Adopted Name (USAN)—a generic, nonproprietary designation. Upon being listed in the United States Pharmacopeia, this nonproprietary name becomes the drug's official name. Additionally, the manufacturer assigns a proprietary name or trademark, which serves as the brand name under which the drug is marketed. It is worth noting that the same...
Drug Control Governance: Regulatory Bodies and Their Impact01:03

Drug Control Governance: Regulatory Bodies and Their Impact

Drug control governance involves the oversight and regulation of pharmaceuticals to ensure their safety and efficacy while preventing illegal drug use and trafficking. Regulatory bodies, including the US Food and Drug Administration (FDA) and the European Union's European Medicines Agency (EMA), play a central role in this process. These agencies evaluate the safety and efficacy of drugs before they can be marketed. They fund clinical trials and assess the benefits and risks associated with a...
Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...

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[Update on the Mali Pharmacy Code: legislative section].

S Maiga1, B Haidara, O Thioune

  • 1FMPOS.

Le Mali Medical
|March 26, 2011
PubMed
Summary
This summary is machine-generated.

Mali

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Last Updated: Jun 3, 2026

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Published on: May 19, 2020

Area of Science:

  • Pharmaceutical Law
  • Health Regulation
  • African Pharmacy History

Context:

  • Malian pharmacy legislation evolved through French colonization (1895-1960) and post-independence reforms.
  • Key historical texts include the 1803 Law, Public Health Code provisions, and 1950s regional orders.
  • Post-colonial Mali adopted and adapted existing laws while introducing new pharmaceutical regulations.

Purpose:

  • To compile and codify all legislative and regulatory texts governing pharmacy in Mali.
  • To examine the historical evolution of pharmacy laws from colonization to the present.
  • To create a unified legal framework for pharmacy practice and education in Mali.

Summary:

  • This work consolidates scattered Malian pharmacy laws, including colonial-era decrees and post-independence statutes.
  • A comprehensive review and codification of legislative texts related to pharmacy and pharmaceutical studies were performed.
  • The resulting code features 189 articles organized into 5 titles, chapters, and sections.

Impact:

  • Provides a unified and accessible legal reference for Malian pharmacy professionals and policymakers.
  • Facilitates understanding and compliance with national pharmaceutical regulations.
  • Establishes a foundational legal structure for the advancement of pharmacy practice and education in Mali.