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Dear friends,

It is with great pleasure that I welcome you to the website of the Pharmaceutical Services of the Ministry of Health. The content of this website is aimed at health professionals as well as pharmaceutical companies and professional societies. The website includes a broad range of information. This includes details on the organisational structure of the Pharmaceutical Services, access to legislation as well as detailed announcements and press releases relating to medicine safety. In addition, the website also includes application forms for all procedures and services, the price list for medicinal products, the formulary of medicines available at the government hospitals, overnight pharmacies etc. In the website, users may also find information for all Councils and Committees of the Pharmaceutical Services as well as their mandates.

It is worth noting that through the e-services module, users can search for registered medicinal products (with the use of key words) and have access to the Product Information Leaflet and other information such as pack sizes, product content, manufacturers etc. An important novelty foreseen for the near future is the implementation of the option for Marketing Authorisation Holders and other applicants to submit their applications in electronic form through the web portal.

The primary objective of the Pharmaceutical Services is to establish a forum for direct communication with the public, associates and stakeholders via the continuous updating and upgrading of our website. It is our desire that the public has access to all useful information relating to matters within our mandate in order to assure a prompt and high quality service.

We wish you a creative and pleasurable navigation at our web site.

Dr Louis Panayi
Director Pharmaceutical Services


















[  Αρχείο Word Sales submission- Private sector
  (Date: 21/03/2014 / Size: 69,35 Kb)


  File Acrobat Reader Reporting requirements of Individual Case Safety Reports (ICSRs) applicable to marketing authorisation holders during the interim period
  (Date: 07/12/2012 / Size: 85,51 Kb)


  File Acrobat Reader Questions and Answers to support the implementation of the Pharmacovigilance legislation - UPDATE, NOVEMBER 2012
  (Date: 07/12/2012 / Size: 282,27 Kb)


  File Acrobat Reader New procedure for the issue/renewal of exceptional marketing authorizations
  (Date: 14/08/2012 / Size: 372,72 Kb)


  Αρχείο Excel LATEST LIST OF APPROVED DRUGS
  (Date: 18/04/2012 / Size: 2465,15 Kb)


  File Acrobat Reader Amended procedure for the electronic reporting of adverse reactions (ICSRs) to the Cyprus Competent Authority
  (Date: 11/04/2012 / Size: 90,82 Kb)


  Αρχείο Word Submission of data relating to the volume of sales of pharmaceutical products marketed in the Republic of Cyprus
  (Date: 11/04/2012 / Size: 79,04 Kb)


[  Αρχείο Word APPLICATION FORM FOR PATIENTS WHO CARRY CONTROLLED DRUGS DURING THEIR HOLIDAY IN CYPRUS
  (Date: 14/09/2011 / Size: 44,88 Kb)


  Αρχείο Word Repeat Mutual Recognition Procedure (rMRP): Administrative (or Zero Days) Repeat MRP with Cyprus as the only CMS
  (Date: 30/08/2011 / Size: 91,79 Kb)


  Αρχείο Word Circular: Simplification of Renewal Procedure for National Medicinal Products that have Undergone at Least One 5year Renewal
  (Date: 10/01/2011 / Size: 135,14 Kb)


  Αρχείο Word Circular: Information for Medicinal Products Authorised through the Centralised Procedure
  (Date: 10/01/2011 / Size: 96,89 Kb)


  Αρχείο Word GUIDANCE FOR PROVIDING REGULATORY INFORMATION IN ELECTRONIC FORMAT SUBMISSIONS
  (Date: 12/11/2009 / Size: 161,15 Kb)


  File Acrobat Reader Pharmacovigilance reporting requirements
  (Date: 03/09/2008 / Size: 59,65 Kb)


  File Acrobat Reader NEW VERSION OF CHAPTER 7 - NOTICE TO APPLICANTS
  (Date: 31/07/2007 / Size: 678,24 Kb)


Product Safety

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