Algeria: Ministry of Health, Population and Hospital Reform

Direction Générale de la Pharmacie et des Equipements de Santé

http://www.sante.dz/

Algeria’s Directorate General of Pharmacy And Health Facilities publish status of registered drugs in downloadable formats (pdf) and it is well managed for each registered product. Complete information of each product is given. Database is easy to understand.

http://www.sante.dz/nomenclaure_26_06_2016.pdf

Algerian authority also provides the Expected needs in pharmaceuticals. Current it is available for the year - 2016.
http://www.sante.dz/prevision_prod_pharm_2016.htm

Websites also provide the Local manufacture of Medicines, currently the following database are available on the database.

Status of achievements

• Year 2012 - - Year 2013
• Year 2010 - - Year 2011

Language: French

Pricing: pricing of the drugs are not available on the online database.

Published registered drug database provides the following results of each product.

• S. No
• ATC Code
• Name of API, Active Pharmaceutical ingredient
• Brand Name / trade Name
• Pharmaceutical form
• Dosage
• Packaging
• Category
• HOS/ private
• LABORATORIES/ Manufacturer
• HOLDER OF THE/ country
• Date of Registration
• Generic/ Branded
• Status
• Shelf life

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Uganda: National Drug Authority (NDA) - Drug Register

National Drug Authority (NDA)

http://www.nda.or.ug/#

Online database is well managed each product information in each category are given online. Database is easy to understand. Information is available under the tab of “Drug register” on the website interface. Monthly registration database of each below mentioned categories can be downloaded in .pdf file under the section of “Downloads”.

Drug Register
This list is updated regularly when available data on such products are evaluated and relevant sites are inspected by National Drug Authority. Please enter the criteria below to display products from the Drug Register database.

This database provides the online list on the following categories.

• Dietary
• Health
• Herbal Human
• Herbal Vet
• Human
• Veterinary

Language: English

Pricing: pricing of the drugs are not available on the online database.

Online database provides the following results of each product.

• Serial Number
• Manufacturer
• Drug Name
• Number
• Pack Sizes
• Dosage Form
• Applicant
• Country of Origin
• Importer

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EudraPharma Database- A complete & Updated Registered Drug Database of whole Europe.

EudraPharma Database

EudraPharm Database is a complete data repository of whole Europe's registered drugs for Human & Veterinary drugs can be found in complete EU including UK.

About EudraPharm
EudraPharm is intended to be a source of information on all medicinal products for human or veterinary use that have been authorised in the European Union (EU) and the European Economic Area (EEA) and information on clinical trials of medicinal products including products with or without a marketing authorization. EudraPharm has been established to fulfil Articles 57(1)(l) and 57(2) of Regulation (EC) No 726/2004.

Use of this site is subject to terms and conditions specified on the EudraPharm Notices page, which also contains Copyright and Privacy Policy information. 

Languages
EudraPharm is available in the following languages:
Bulgarian, Spanish, Czech, Danish, German, Estonian, Greek, English, French, Icelandic, Italian, Latvian, Lithuanian, Hungarian, Maltese, Dutch, Norwegian, Polish, Portuguese, Romanian, Slovak, Slovenian, Finnish, Swedish

Withdrawn Products
Companies sometimes withdraw medicines from the market, and they surrender their marketing authorisation. In such cases, EudraPharm may not show any details for the presentation or the product.

Current Functionality
EudraPharm currently provides the following functionality:

Display product information for all products approved via the Centralised Procedure, as well as for some products approved via national procedures (see Data Providers).

Display Product-Information Documents for all products approved via the Centralised Procedure. The documents contain Summary of Product Characteristics, Package Leaflet and Labelling information.

Search - find product by searching for a set category of product information. 

A to Z Product List - browse product details indexed alphabetically by Product Name. 

Advanced Search - find product by searching for specific categories of product information. 

Access to data on clinical trials - EU Clinical Trials Register.

EudraPharm is being developed in stages. Therefore, the functionality and related support will increase in future.

Future Functionality
The following functionality will be available in the future:

• Ability to search all categories of product information. 
• Ability to register with EudraPharm so that you can set your preferences. 
• Ability to register for e-mail updates. 
• Ability to view warnings and indications. 
• Ability to view product information customised to the requirements of Data Providers. 

EudraPharm Data Providers
The product information contained in EudraPharm is collected from the following Data Providers:
National Competent Authorities.
European Medicines Agency.

Click on the name of the Data Provider listed below to view their website. Please note that:

The EudraPharm Data Providers are not responsible for the content of external websites.
The websites do not necessarily provide product information.
The websites are only provided as a reference for further information about the Data Providers.
If you find that a link is out of date, or broken, you are invited to e-mail the EudraPharm Helpdesk to allow us to rectify the issue: <eudrapharm@ema.europa.eu>

Product information from the following Data Providers can currently be viewed in EudraPharm: 

Country/Body
EudraPharm Data Provider
European Union (EU)
European Medicines Agency

Ireland
Health Products Regulatory Authority
Italy
Ministero della Salute

Latvia
Zāļu valsts aģentūra
Netherlands
College ter Beoordeling van Geneesmiddelen

Portugal
INFARMED - Autoridade Nacional do Medicamento e Produtos de Saúde, I.P. 

United Kingdom
Veterinary Medicines Directorate

France
Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail – ANSES (Agence nationale du médicament vétérinaire - ANMV)
It is planned to include product information from the following Data Providers in the future:
Country/Body
EudraPharm Data Provider

Austria
Agentur für Gesundheit und Ernährungssicherheit - AGES

Belgium
Agence Fédérale des Médicaments et des Produits de Santé - AFMPS
Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten - FAGG
Föderale Agentur für Arzneimittel und Gesundheitsprodukte - FAAG 

Bulgaria
Изпълнителна агенция по лекарствата
Национална ветеринарномедицинска служба
Cyprus
Υπουργείο Γεωργίας, Φυσικών Πόρων και Περιβάλλοντος (Κτηνιατρικές Υπηρεσίες)
Υπουργείο Υγείας της Κυπριακής Δημοκρατίας

Czech Republic
Státní ústav pro kontrolu léčiv
Ústav pro státní kontrolu veterinárních biopreparátů a léčiv

Germany
Bundesamt für Verbraucherschutz und Lebensmittelsicherheit - BVL
Bundesinstitut für Arzneimittel und Medizinprodukte - BfArM
Deutsches Institut für Medizinische Dokumentation und Information - DIMDI
Paul-Ehrlich-Institut - PEI

Denmark
Lægemiddelstyrelsen

Estonia
Ravimiamet
Greece
Εθνικός Οργανισμός Φαρμάκων - EOF
Spain
Agencia Española de Medicamentos y Productos Sanitarios - AGEMED

Finland
Lääkealan turvallisuus- ja kehittämiskeskus

France
Agence Française de Sécurité Sanitaire des Produits de Santé - AFSSAPS

Hungary
Mezőgazdasági Szakigazgatási Hivatal Központ Állatgyógyászati Termékek Igazgatósága - MgSzH ÁTI
Országos Gyógyszerészeti Intézet
Iceland
Lyfjastofnun
Italy
Agenzia Italiana del Farmaco - AIFA
Istituto Superiore di Sanità

Liechtenstein
Amt für Gesundheit

Lithuania Lietuvos Respublikos Valstybinè Maisto ir Veterinarijos Tarnyba
Valstybine vaistu kontroles tarnyba prie Lietuvos Respublikos sveikatos apsaugos ministerijos

Luxembourg
Ministère de la Santé, Direction de la Santé, Division de la Pharmacie et des Médicaments

Malta
Medicines Authority
Ministry for Rural Affairs and the Environment

Norway
Statens legemiddelverk

Poland
Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych

Portugal
Direcção Geral de Veterinária - DGV

Romania
Agentia Nationala a Medicamentului - ANM
Autoritatea Nationala Sanitara Veterinara si pentru Siguranta Alimentelor - ANSVSA

Sweden
Läkemedelsverket

Slovenia
Javna agencija Republike Slovenije za zdravila in medicinske pripomočke

Slovakia
Štátny ústav pre kontrolu liečiv - ŠÚKL
Ústav štátnej kontroly veterinárnych biopreparátov a liečiv

United Kingdom
Medicines and Healthcare products Regulatory Agency - MHRA

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Sofosbuvir Pricing

Rapid reductions in prices for generic sofosbuvir and daclatasvir to treat hepatitis C

Andrew Hill, 1 Bryony Simmons, 2 Dzintars Gotham, 2 and Joseph Fortunak 3

Author information ► Copyright and License information ►

Abstract
Objectives:
Novel treatments for hepatitis C demonstrate high cure rates, but current high prices can be a barrier to rapid global treatment scale-up. Generic competition can rapidly lower drug prices. Using data on exports of raw materials in 2015, we calculated currently feasible generic prices of sofosbuvir and daclatasvir.

Methods:
Data on per-kilogram prices of sofosbuvir and daclatasvir active pharmaceutical ingredients (API) exported from India were extracted from an online database. To the cost of the amount of API needed for a 12-week treatment course, we added cost estimates for formulation (40%), packaging (US$0.35/month), and a mark-up (50%).

Results:
Between 1 January and 15 October 2015, over 5 tons of sofosbuvir were exported, with prices decreasing by US$702/kg/month, and observed prices of US$2501/kg in early September. Over the same period, 84 kg of daclatasvir were exported, with prices decreasing by US$1664/kg/month to US$1897/kg. Using the price estimation algorithm, we estimated the price of a generic sofosbuvir–daclatasvir combination regimen at US$200 per patient for a 12-week treatment course.

Conclusion:
The costs of generic production of sofosbuvir and daclatasvir are rapidly decreasing. Sofosbuvir–daclatasvir combination treatment could be produced for US$200 per patient per 12-week course.

Download link

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Panama: Ministry of Health-List of Drugs in the process of Sanitary Registration

Ministry of Health, Panama

List of Drugs in the process of Sanitary Registration

Panama MoH although publish the registered drug database and they are also available on the Panama MoH website but the database is not updated till,date. However,can be downloaded for the year 2012, 2013, and 2014.

Information on registered drugs is available of registered products till 2014. The drug regulatory departments have the following documents available.

Pricing is not available in the MoH Database

Language: Spanish

List of Drugs in the process of Health Registration 2014

List of Drugs in the process of Sanitary Registration (01 Jul - 15 Jul)
List of Drugs in the process of Sanitary Registration (June 16 - June 30)
List of Drugs in the process of Sanitary Registration (01 Jun - 15 Jun.)
List of Drugs in the process of Sanitary Registration (May 16 - May 31)
List of Medicines in the process of Sanitary Registration (01 May - 15 May.)
List of Medicines in the process of Health Registration (Apr 16 - Apr 30)
List of Medicines in the process of Health Registration (01 Apr - 15 Apr)
List of Medicines in the process of Sanitary Registration (16 Mar. - 31 Mar.)
List of Drugs in the process of Sanitary Registration (01 Mar. - 15 Mar.)
List of Drugs in the process of Sanitary Registration (Feb. 16 - Feb. 28)
List of Drugs in the process of Sanitary Registration (01 Feb. - 15 Feb.)
List of Drugs in the process of Health Registration (Jan 16 - Jan 31)
List of Drugs in the process of Sanitary Registration (01 Jan. - 15 Jan.)



List of Medicines in the process of Sanitary Registration 2013

List of Medicines in the process of Health Registration (Dec 16 - Dec 31)
List of Drugs in the process of Health Registration (Dec 01 - Dec 15)
List of Drugs in the process of Sanitary Registration (16 Nov. - 30 Nov.)
List of Medicines in process of Sanitary Registration (01 Nov. - 15 Nov.)
List of Medicines in the process of Sanitary Registration (Oct. 16 - Oct. 31)
List of Medicines in the process of Sanitary Registration (01 Oct. - 15 Oct.)
List of Drugs in the process of Sanitary Registration (16 Sep. - 30 Sep.)
List of Medicines in the process of Sanitary Registration (01 Sep. - 15 Sep.)
List of Drugs in the process of Sanitary Registration (16 Aug - 31 Aug)
List of Drugs in the process of Sanitary Registration (01 Aug - 15 Aug)
List of Drugs in the process of Health Registration (July 16 - July 31)
List of Drugs in the process of Sanitary Registration (01 Jul - 15 Jul)
List of Drugs in the process of Sanitary Registration (01 Jun - 30 Jun.)
List of Medicines in the process of Sanitary Registration (01 May - 31 May)
List of Medicines in the process of Sanitary Registration (06 Abr. - 30 Abr.)
List of Drugs in the process of Sanitary Registration (16 Mar. - 05 Abr.)
List of Medicines in the process of Sanitary Registration (15 Feb. - 15 Mar.)
List of Drugs in the process of Health Registration (Jan 16 - Feb 14)
List of Drugs in the process of Sanitary Registration (01 Jan. - 15 Jan.)



List of Medicines in process of Sanitary Registration 2012

List of Drugs in the process of Sanitary Registration (30 Nov.- 31 Dec.)
List of Drugs in the process of Sanitary Registration (Nov.- Nov. 29)
Of Medicines in the process of Health Registry (03 Nov.- 16 Nov.)
List of Drugs in the process of Sanitary Registration (20 Oct.-02 Nov.)
List of Medicines in the process of Sanitary Registration (13-19 Oct.)
List of Medicines in the process of Health Registration (06-12 Oct.)
List of Medicines in the process of Sanitary Registration (29-05 Oct.)
List of Medicines in the process of Sanitary Registration (22-28 Sept.)
List of Medicines in the process of Sanitary Registration (15-21 Sept.)

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