This regulation establishes the rules applicable to the exercise of pharmaceutical activity, in the public and private sectors, by natural or legal persons.
This law establishes the rules relating to medicines, other health products and pharmacy.
This decree regulates the exercise of hospital pharmaceutical activity in the health structures of the National Health Service. It covers all health structures of the National Health Service that carry out this activity, namely central hospitals and regional hospitals. Its purpose is to organize, improve, optimize and standardize hospital pharmaceutical services in the National Health Service.
The law establishes the Pharmacy Council of Nigeria and regulates the standard of training and practice of pharmacy.
These Instructions govern private health facilities.
The Regulation sets up rules in the registration of drugs and related products manufactured, imported, exported, advertised, sold, distributed or used in Nigeria.
The legislation regulates the production, import, export, conservation, distribution, quality analysis and sale of medicines for human use, including traditional medicines, as well as all other health products, pharmaceutical practice and opticianry.
Specifications for essential medicines supplies.
The instructions govern dual clinical practice in Rwanda. The Instructions apply to medical doctors and dental surgeons working in health facilities.
Ministerial instructions No 20/003 of 23/09/2020 governing private health facilities in Rwanda
The Instructions are intended to improve the quality of health care services provided in private health facilities to the Rwandan population and to determine the basic requirements for the operation of a private health facility. These instructions do not regulate traditional, alternative and complementary medicine.
These Regulations provide rules on the registration and access to the market to medicine; licensing requirements for pharmaceutical operations, manufacturers, wholesalers and dispensaries; as well as on record-keeping, import of medicines, and clinical trials, etc.
This Decree creates and establishes the rules for the organization and operation of the National Order of Pharmacists of Mauritania (ONPM). This Decree is published in a collection of other legislative acts and can be found on page 10 of the file.
The document establishes the standards for the authorization to operate a private health facility in Rwanda.
The law regulates the manufacture and registration of medicines, the approval of medical devices, and sets out rules for pharmacies and the practice of the profession of pharmacist.
The Decree creates a Code of Ethics for pharmacists in Mali. The Code is applicable to all pharmacists who meet the legal and regulatory requirements and are registered with the Ordre des Pharmaciens (Order of Pharmacists). The Code sets out, among other things, the requirements and duties associated with the practice of the profession.
The law creates the Ordre des Pharmaciens (The Order of Pharmacists), which is responsible for organizing and representing individuals and legal entities practicing the pharmaceutical professions in Mali.
The decree sets out the organization and operating procedures for hospital pharmacies.
Lei No 12/2017 Lei de medicamento, vacinas e outros produtos biológicos para o uso humano
This Law establishes the rules for the efficient and safe production, distribution, use and availability, as well as quality assurance of medicines, vaccines, biological and health products for citizens.
This document describes for each level of care, the types of services offered, the description and qualifications of the staff that provide the services and the equipment required to carry out the services. The health service packages support the clinical and managerial standards by which the healthcare facilities operate. The ultimate goal of this document is to provide guidance in the organization of private health service facilities to improve the quality of health care and services provided to the population of Rwanda.
These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.