Топ-100
  • Side Effects (2005 film) Side Effects (2005 film)

    Side Effects is a 2005 romantic comedy about the pharmaceutical industry, directed by Kathleen Slattery-Moschkau and starring Katherine Heigl as Karly Hert, ...

  • Prescription Drug User Fee Act Prescription Drug User Fee Act

    The Prescription Drug User Fee Act was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration to collect fees from...

  • Prescription Drug Marketing Act Prescription Drug Marketing Act

    The Prescription Drug Marketing Act of 1987 is a law of the United States federal government. It establishes legal safeguards for prescription drug distribut...

  • Pharmaceutical Press Pharmaceutical Press

    Pharmaceutical Press is the publishing arm of the Royal Pharmaceutical Society. It is a provider of independent pharmaceutical information. Its principal pub...

  • Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme

    The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme are two international instruments between countries and pharmaceut...

  • Pharmaceutical fraud Pharmaceutical fraud

    Pharmaceutical fraud involves activities that result in false claims to insurers or programs such as Medicare in the United States or equivalent state progra...

  • Orphan Drug Act of 1983 Orphan Drug Act of 1983

    The Orphan Drug Act of 1983 is a law passed in the United States to facilitate development of orphan drugs - drugs for rare diseases such as Huntingtons dise...

  • NPS MedicineWise NPS MedicineWise

    Established in March 1998, NPS MedicineWise is an Australian not-for-profit organisation whose programs are funded by the national Department of Health. Sinc...

  • No Free Lunch (organization) No Free Lunch (organization)

    No Free Lunch was a US-based advocacy organization holding that marketing methods employed by drug companies influence the way doctors and other healthcare p...

  • Multi-drug-resistant tuberculosis Multi-drug-resistant tuberculosis

    Multi-drug-resistant tuberculosis is a form of tuberculosis infection caused by bacteria that are resistant to treatment with at least two of the most powerf...

  • MIMS Ireland MIMS Ireland

    The Monthly Index of Medical Specialities Ireland is a well-established prescribing guide delivered to medical practitioners in Ireland. It was founded by Dr...

  • Medicare Prescription Drug, Improvement, and Modernization Act Medicare Prescription Drug, Improvement, and Modernization Act

    The Medicare Prescription Drug, Improvement, and Modernization Act, also called the Medicare Modernization Act or MMA, is a federal law of the United States,...

  • Medicare Part D Medicare Part D

    Medicare Part D, also called the Medicare prescription drug benefit, is an optional United States federal-government program to help Medicare beneficiaries p...

  • Medical cannabis Medical cannabis

    Medical cannabis, or medical marijuana, is cannabis and cannabinoids that are prescribed by physicians for their patients. The use of cannabis as medicine ha...

  • Marketing authorization Marketing authorization

    Marketing authorisation is the process of reviewing and assessing the evidence to support a medicinal product, such as a drug, in relation to its marketing, ...

  • Kefauver Harris Amendment Kefauver Harris Amendment

    The U.S. Kefauver Harris Amendment or "Drug Efficacy Amendment" is a 1962 amendment to the Federal Food, Drug, and Cosmetic Act. It introduced a requirement ...

  • Food and Drug Administration Modernization Act of 1997 Food and Drug Administration Modernization Act of 1997

    The United States Food and Drug Administration Modernization Act of 1997 amended the Federal Food, Drug, and Cosmetic Act. This act is related to the regulat...

  • Durham-Humphrey Amendment Durham-Humphrey Amendment

    The Durham-Humphrey Amendment explicitly defined two specific categories for medications, legend and over-the-counter. This amendment was co-sponsored by the...

  • Drug utilization review Drug utilization review

    Drug utilization review refers to a review of prescribing, dispensing, administering and ingesting of medication. This authorized, structured and ongoing rev...

  • Drug Quality and Security Act Drug Quality and Security Act

    The Drug Quality and Security Act is a law that amended the Federal Food, Drug, and Cosmetic Act to grant the Food and Drug Administration more authority to ...

  • Drug nomenclature Drug nomenclature

    Drug nomenclature is the systematic naming of drugs, especially pharmaceutical drugs. In the majority of circumstances, drugs have 3 types of names: chemical...

  • Contract research organization Contract research organization

    A contract research organization is a company that provides support to the pharmaceutical, biotechnology, and medical device industries in the form of resear...

  • The Constant Gardener The Constant Gardener

    The Constant Gardener is a 2001 novel by British author John le Carre. The novel tells the story of Justin Quayle, a British diplomat whose activist wife is ...

  • Clinical Trials Directive Clinical Trials Directive

    The Clinical Trials Directive is a European Union directive that aimed at facilitating the internal market in medicinal products within the European Union, w...

  • British National Formulary for Children British National Formulary for Children

    The British National Formulary for Children is the standard UK paediatric reference for prescribing and pharmacology, among others indications, side effects ...

  • Authorized generics Authorized generics

    Authorized generics are prescription drugs produced by brand pharmaceutical companies and marketed under a private label, at generic prices. Authorized gener...

  • Access to Cannabis for Medical Purposes Regulations Access to Cannabis for Medical Purposes Regulations

    The Marihuana for Medical Purposes Regulations was a set of Canadian regulations enacted in July 2013 concerning the production, distribution and use of medi...

  • 2006 Oregon Ballot Measure 44 2006 Oregon Ballot Measure 44

    Oregon ballot measure 44 was an initiated state statute ballot measure on the November 7, 2006 general election ballot. The Measure modified the eligibility ...

  • Pharmaceutical policy Pharmaceutical policy

    Pharmaceutical policy is a branch of health policy that deals with the development, provision and use of medications within a health care system. It embraces...

Pharmaceutical policy

Pharmaceutical policy is a branch of health policy that deals with the development, provision and use of medications within a health care system. It embraces...

2006 Oregon Ballot Measure 44

Oregon ballot measure 44 was an initiated state statute ballot measure on the November 7, 2006 general election ballot. The Measure modified the eligibility ...

Access to Cannabis for Medical Purposes Regulations

The Marihuana for Medical Purposes Regulations was a set of Canadian regulations enacted in July 2013 concerning the production, distribution and use of medi...

American Society of Pharmacognosy

The American Society of Pharmacognosy is a scientific society that promotes the growth and development of pharmacognosy through presentation of research achi...

Authorized generics

Authorized generics are prescription drugs produced by brand pharmaceutical companies and marketed under a private label, at generic prices. Authorized gener...

Seneka Bibile

Prof. Senaka Bibile was a Sri Lankan pharmacologist. He was the founder of Sri Lankas drug policy, which was used as a model for development of policies base...

NHS treatments blacklist

The NHS treatments blacklist is an informal name for a list of medicines and procedures which will not be funded by public money except in exceptional cases....

British National Formulary for Children

The British National Formulary for Children is the standard UK paediatric reference for prescribing and pharmacology, among others indications, side effects ...

Canada's Access to Medicines Regime

Canadas Access to Medicines Regime is a process established by the Canadian government that allows Canada to enact compulsory licenses to export essential me...

Canadian Agency for Drugs and Technologies in Health

The Canadian Agency for Drugs and Technologies in Health, or CADTH, is a Canadian national organisation that provides research and analysis to healthcare dec...

Certificate of pharmaceutical product

The certificate of pharmaceutical product is a certificate issued in the format recommended by the World Health Organization, which establishes the status of...

Clinical Trials Directive

The Clinical Trials Directive is a European Union directive that aimed at facilitating the internal market in medicinal products within the European Union, w...

The Constant Gardener

The Constant Gardener is a 2001 novel by British author John le Carre. The novel tells the story of Justin Quayle, a British diplomat whose activist wife is ...

Contract research organization

A contract research organization is a company that provides support to the pharmaceutical, biotechnology, and medical device industries in the form of resear...

Council for International Organizations of Medical Sciences

The mission of the Council for International Organizations of Medical Sciences is to advance public health through guidance on health research including ethi...

Directive 75/318/EEC

Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards a...

Directive 75/319/EEC

Directive 75/319/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards a...

Medicare Part D coverage gap

The Medicare Part D coverage gap is a period of consumer payment for prescription medication costs which lies between the initial coverage limit and the cata...

Drug Efficacy Study Implementation

Drug Efficacy Study Implementation was a program begun by the Food and Drug Administration in the 1960s after the requirement that all drugs be efficacious a...

Drug nomenclature

Drug nomenclature is the systematic naming of drugs, especially pharmaceutical drugs. In the majority of circumstances, drugs have 3 types of names: chemical...

Drug Quality and Security Act

The Drug Quality and Security Act is a law that amended the Federal Food, Drug, and Cosmetic Act to grant the Food and Drug Administration more authority to ...

Drug utilization review

Drug utilization review refers to a review of prescribing, dispensing, administering and ingesting of medication. This authorized, structured and ongoing rev...

Durham-Humphrey Amendment

The Durham-Humphrey Amendment explicitly defined two specific categories for medications, legend and over-the-counter. This amendment was co-sponsored by the...

EudraGMP

EudraGMP is the database of the European Community of manufacturing authorisations and of certificates of good manufacturing practice. The EudraGMP system wa...

EUDRANET

EUDRANET, the European Telecommunication Network in Pharmaceuticals, is an IT platform to facilitate the exchange of information between regulatory partners ...

EuroPharm Forum

The EuroPharm Forum was a network of national pharmaceutical associations in Europe, in collaboration with the World Health Organization Regional Office for ...

First Databank

First Databank is a major provider of drug and medical device databases that help healthcare professionals make precise decisions. FDB partners with informat...

Food and Drug Administration Modernization Act of 1997

The United States Food and Drug Administration Modernization Act of 1997 amended the Federal Food, Drug, and Cosmetic Act. This act is related to the regulat...

International Society for Pharmacoepidemiology

The International Society for Pharmacoepidemiology was launched officially by Stanley A. Edlavitch, David E. Lilienfeld, and Hugh A. Tilson in 1989 during th...

International Society of Pharmacovigilance

The International Society of Pharmacovigilance, previously the European Society of Pharmacovigilance, is an international non-profit scientific organisation,...

International Union of Basic and Clinical Pharmacology

The International Union of Basic and Clinical Pharmacology is a voluntary, non-profit association representing the interests of scientists in pharmacology-re...

IPLEDGE program

The iPLEDGE program is a risk management distribution program mandated by the U.S. Food and Drug Administration for isotretinoin, marketed as Absorica, Clara...

Kefauver Harris Amendment

The U.S. Kefauver Harris Amendment or "Drug Efficacy Amendment" is a 1962 amendment to the Federal Food, Drug, and Cosmetic Act. It introduced a requirement ...

KwikMed

KwikMed is an approved online pharmacy in the United States which has been granted regulatory approval to operate and sell medications online. Based in Salt ...

LegitScript

LegitScript is a Portland, Oregon-based internet and payments compliance company that provides solutions for merchant monitoring, platform monitoring, and ce...

Marketing authorization

Marketing authorisation is the process of reviewing and assessing the evidence to support a medicinal product, such as a drug, in relation to its marketing, ...

Medical cannabis

Medical cannabis, or medical marijuana, is cannabis and cannabinoids that are prescribed by physicians for their patients. The use of cannabis as medicine ha...

Medicare Part D

Medicare Part D, also called the Medicare prescription drug benefit, is an optional United States federal-government program to help Medicare beneficiaries p...

Medicare Prescription Drug, Improvement, and Modernization Act

The Medicare Prescription Drug, Improvement, and Modernization Act, also called the Medicare Modernization Act or MMA, is a federal law of the United States,...

Medicines Act 1968

The Medicines Act 1968 is an Act of Parliament of the United Kingdom. It governs the control of medicines for human use and for veterinary use, which include...

MIMS Ireland

The Monthly Index of Medical Specialities Ireland is a well-established prescribing guide delivered to medical practitioners in Ireland. It was founded by Dr...

Multi-drug-resistant tuberculosis

Multi-drug-resistant tuberculosis is a form of tuberculosis infection caused by bacteria that are resistant to treatment with at least two of the most powerf...

Essential medicines policies

An essential medicines policy is one that aims at ensuring that people get good quality drugs at the lowest possible price, and that doctors prescribe the mi...

No Free Lunch (organization)

No Free Lunch was a US-based advocacy organization holding that marketing methods employed by drug companies influence the way doctors and other healthcare p...

NPS MedicineWise

Established in March 1998, NPS MedicineWise is an Australian not-for-profit organisation whose programs are funded by the national Department of Health. Sinc...

Ohio Automated Rx Reporting System

The Ohio Automated Rx Reporting System is Ohios state Prescription Monitoring Program and is controlled by the Ohio State Board of Pharmacy. The law permitti...

Orphan Drug Act of 1983

The Orphan Drug Act of 1983 is a law passed in the United States to facilitate development of orphan drugs - drugs for rare diseases such as Huntingtons dise...

2012 Pakistan fake medicine crisis

During late January 2012, a fake medicine crisis at the Punjab Institute of Cardiology hospital in the Lahore region of Punjab, Pakistan, claimed the lives o...

Patient Group Directions

Patient Group Directions are documents in the U.K. National Health Service that permit the supply of prescription-only medicines to groups of patients, witho...

Pharmac

The Pharmaceutical Management Agency, better known as Pharmac, is a New Zealand Crown entity that decides, on behalf of District Health Boards, which medicin...

Pharmaceutical Benefits Scheme

The Pharmaceutical Benefits Scheme is a program of the Australian Government that provides subsidised prescription drugs to residents of Australia, as well a...

Pharmaceutical fraud

Pharmaceutical fraud involves activities that result in false claims to insurers or programs such as Medicare in the United States or equivalent state progra...

Pharmaceutical industry in China

The pharmaceutical industry is one of the leading industries in the Peoples Republic of China, covering synthetic chemicals and drugs, prepared Chinese medic...

Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme

The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme are two international instruments between countries and pharmaceut...

Pharmaceutical Press

Pharmaceutical Press is the publishing arm of the Royal Pharmaceutical Society. It is a provider of independent pharmaceutical information. Its principal pub...

Pharmaceutical Price Regulation Scheme

The Pharmaceutical Price Regulation Scheme is the mechanism used by the UK Department of Health to ensure that the NHS has access to good quality branded med...

Postmarketing surveillance

Postmarketing surveillance is the practice of monitoring the safety of a pharmaceutical drug or medical device after it has been released on the market and i...

Prescription Drug Marketing Act

The Prescription Drug Marketing Act of 1987 is a law of the United States federal government. It establishes legal safeguards for prescription drug distribut...

Prescription Drug User Fee Act

The Prescription Drug User Fee Act was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration to collect fees from...

Prescription monitoring program

In the United States, prescription monitoring programs or prescription drug monitoring programs are state-run programs which collect and distribute data abou...

Qualified person (European Union)

Qualified person is a technical term used in European Union pharmaceutical regulation. The regulations specify that no batch of medicinal product can be rele...

The Rhetoric of Drugs

The Rhetoric of Drugs in the original French title, is a 1990 work by French philosopher Jacques Derrida. Derrida, interviewed, discusses the concept of "dru...

Side Effects (2005 film)

Side Effects is a 2005 romantic comedy about the pharmaceutical industry, directed by Kathleen Slattery-Moschkau and starring Katherine Heigl as Karly Hert, ...

Society of Pharmacovigilance, India

The Society of Pharmacovigilance, India, is an Indian national non-profit scientific organisation, which aims at organizing training programmes and providing...