FarmavitaR+

regulatory affairs network

  • Increase font size
  • Default font size
  • Decrease font size
Regulatory Affairs

Introduction of Braille script for pharmaceuticals in Ukraine

E-mail Print PDF

Braille script

20.05.2009 was introduced an amendment to the law of Ukraine “On medicines” (№ 124/96ВР of 4.04.96) which orders to use Braille script on packages. Changes came into force until 01.01.10. In Ukraine live approximately 45 000 of semi-blind people and 10 000 – 20 000 from this number are totally blind.

Read more...
 

Regulatory Updates - Free Webinar Series

E-mail Print PDF

Free Webinar Series

In order to fulfill dicentra’s mission to serve the natural health products industry as a source for education and trusted scientific and regulatory information, we offer free quarterly regulatory updates (every 3 months) through an online webinar.


These webinars are meant to keep you and all of your fellow coworkers up-to-date on the latest issues pertaining to scientific and regulatory affairs. The main focus of each webinar will be for anything important pertaining to natural health products and their regulations in Canada. Examples include a summary of the Natural Health Products Directorate’s status of submissions reports, the latest regulatory status of ingredients, new published monographs, and all other important issues. We will also cover major issues related to other product categories that may have an effect on natural health products.

All webinars are presented by a qualified member of our team and will last approximately 30 minutes. Please register by filling out the form below. Instructions on how to join will be sent to you a day prior to the webinar. Sit back and enjoy our interpretation and navigation to help propel your business forward at no cost.

To register, please visit http://www.dicentra.ca/updates/

 

Act on Medical Products and Medical Devices

E-mail Print PDF

the_law_by_limaoscarjuliet.jpg

Bosnia and Herzegovina-Act on Medical Products and Medical Devices

On May 1st 2009 the Agency for medical products and medical devices in Bosnia and Herzegovina has started with work. The Act on Medical Products and Medical Devices defines Agency's jurisdiction, how to apply for MA in Bosnia and Herzegovina, documentation for registration, pharmacovigilance, advertising...

The law is available for download at Downloads section of Farmavitar.Net. (in Bosnian!)

Read more...
 

Variations

E-mail Print PDF

lemon_by_austintx.jpg

Variations to the terms of medicinal products registered in Albania

This file will explain you how to apply for variation to the trems of medical products and in short a procedure for revocation of marketing authorisation.

The whole 10 pages article is available for download at Downloads section of Farmavitar.Net

Read more...
 

The Food Supplements Registration in Albania

E-mail Print PDF

tablet_by_310875.jpg

REGULATION FOR THE FOOD SUPPLEMENTS REGISTRATION IN THE REPUBLIC OF ALBANIA

The Regulation for Food Supplements Registration  is implemented for the food supplements which are introduced and marketed as alimentary products in the Republic of Albania.

Read more...
 


Page 3 of 13
Banner


Login With Facebook

Regulatory Network

Members : 954
Content : 235
Web Links : 5
Content View Hits : 653173

Who's Online

We have 387 guests online

Featured Partners

Regulanet - regulatory affairs consortium

regulanet®: Local representation for Global Regulatory Affairs

 

Tarius - Regulatory Intelligence Databases

Farmavita.Net - pharmaceutical lisensing network

Pharmaceutical Licensing and technology transfer

 

Authnetic and secured web site

 

Increase your website traffic with Attracta.com


Featured Event

Famavita_150x150_mobile_pharma

Featured Event

bals115_150x150

Featured Event

KSLS08_150x150


Active Groups

{captcha}