Requirements for nomination of a pharmacovigilance (PV) contact person at national level in Lithuania, Latvia, Estonia
Contact persons for PV issues at national level are typically required to speak local language and to reside within the given Member State. Also they should have a direct reporting link to the EU-QPPV...
CPhI Worldwide 2018
BalticCRO will be attending the CPhI Worldwide 2018 taking place between 9th and 11th of October in Madrid, Spain. We look forward to meeting pharmaceutical manufacturers, distributors and service providers, who are interested to learn how we help the industry bring medicinal products to market in faster and smoother. Contact us...
Life Sciences Baltics
We will be attending the Life Sciences Baltics conference and exhibition on September 26-27, 2018 in Vilnius. We look forward to meeting you at the event!
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.