Patient safety is the ultimate objective of any pharmacovigilance (PV) or drug safety department. The appropriate number of qualified, trained personnel are needed to ensure quality pharmacovigilance processes and outcomes…
Standard operating procedures, or SOPs, are quality documents critical to any pharmacovigilance (PV) quality system. Experienced PV professionals need to dedicate time and diligence to ensure these documents are clear, concise, and…
We are a partner at #WODCUSA, the most comprehensive gathering of rare disease stakeholders ever, happening this August 25-27 at the Gaylord National Harbor Hotel. Won’t you join us?
Med Communications can help you start up your standard response database from scratch or manage your existing database. Our seasoned writers are scientifically trained and can lead your strategy development,…
As we prepare for the long holiday weekend in the US, let’s not forget the sacrifices of those who fought for our country. We are a veteran-founded business, so we…
Testimonials such as this one from a top 10 pharmaceutical company offer a testament to our level of service excellence.
One of the primary causes of drug safety inspection findings include non-compliance of spontaneous adverse drug reaction reporting?
Our experienced medical writers create, update, and review all types of slide decks.
Med Communications is happy to partner with the World Orphan Drug Congress this year.
In the latest MHRA GPvP Inspection Metrics Report, risk management comes up as a critical finding. For more information, see post.
