DDReg develop Regulatory Strategies, provide expert Regulatory advice right from product development stage upto launch, dossiers compilation & publishing, post approval market maintenance. Besides Regulatory services DDReg offer a complete range of Pharmacovigilance and Medical Writing services to its clients. At DDReg we manage a Regulatory Affairs or Pharmacovigilance project regardless of size and timescale. From filing submissions to the more complex management of compliance issues, post-licensing activities on one side and form Adverse event processing to complicated Signal detection in Pharmacovigilance on the other side, we are the experts and can supply the desired expertise to match any Regulatory Affairs / Pharmacovigilance need – anywhere in the world.
There are many good reasons as to why some of the leading global pharmaceutical organizations prefer DDReg as their partner, the key ones are highlighted as below