Due to the new pharmacovigilance legislation implementation marketing authorisation holders (Pharmaceutical Companies) needs to submit electronic submission of information on medicinal products for human use to the European Medicines Agency.
The format shows the types of information that companies will need to submit to the Agency by the legal deadline of 2 July 2012.
For More Information please clikc here: EMA New format for submission of information on medicines
No comments:
Post a Comment