New law (The Medicines for Human Use (Advanced Therapy Medicinal Products and Miscellaneous Amendments) Regulations 2010 SI No 1882) comes into force on 19th August 2010. The regulations implement EU Regulation EC/1394/2007 concerning licensing and marketing conditions plus patient and product traceability for ATMPs. They also allow price lists for unlicensed medicines to be published and shared.

This entry was posted on Friday, August 20th, 2010 at 4:41 pm and is filed under Law News, Pharmacy News. You can follow any responses to this entry through the RSS 2.0 feed.