EMA (ex EMEA) is performing a pilot phase of what is known as a Product Information Management system (PIM). It is about interactive IT interface for the submission, review and
Russia, as one of largest and most important pharmaceutical markets in the world underwent significant changes of its pharmaceutical regulatory laws. The new law went into effect in September 2010.
Basel (Switzerland), 16.04.2010 - More than 140 participants, senior officials from health, law enforcement and judicial authorities from around 40 states, international organisations and institutions from around the world came together on
20.05.2009 was introduced an amendment to the law of Ukraine “On medicines” (? 124/96?? of 4.04.96) which orders to use Braille script on packages. Changes came into force until 01.01.10.
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
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
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. In the Annex 1
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. FarmavitaR+ brings you a short
FarmavitaR+ brings you a short description of herbal medical products registration procedure in the Republic of Albania. The whole 4 pages article is available for download at Downloads section of
Russia's rapidly growing over-the-counter market offers pharmaceutical companies a chance to expand their business, but its complex regulations and lengthy registration timelines may hinder entry. "Russia is one of the
