Public Data From Article 57 Database to Ease Assessment of Potential Invented Names for Medicinal Products
As of July 2018, the European Medicines Agency (EMA) publishes data from the Article 57 database on all medicines authorised in the European Economic Area (EEA). The database...
NeeS to eCTD deadline for National Procedures is approaching – are your Dossiers ready?
The extended deadline for National Procedures within the eSubmission Roadmap is coming to an end by kick-off of 2019 and NeeS will become a thing of the past...
We are recruiting!
Currently we are looking for an experienced professional to join our team in a Senior Regulatory Affairs Specialist role. You can check the job description an requirements by clicking here, and apply by contacting us at career@balticCRO.com.
Lithuania has adopted amendments to the Pharmaceutical Law
Lithuania has adopted amendments to the Pharmaceutical Law that will help patients receive the drugs they need in a faster, cheaper and more convenient way. The amendment implements the following changes...
Announcement of Office Relocation
nnouncement of Office Relocation We would like to inform that we have just moved to a new office location on 1st of May 2018. Our new office address is Jonavos g. 30, Kaunas 44262, Lithuania. The new and larger space office location allows us to add more functions in order for value added service to all our customers...
Amendments to the Procedure for Registration of Medicinal Products That Came into Force on 13 April 2018
We would like to inform you, that amendments to the Cabinet of Ministers Regulation No 376 of 9 May 2006 “Procedure for Registration of Medicinal Products” came into force in Latvia on 13 April 2018. The amendments specify the...