09.19.16
Veristat, a full service clinical research organization (CRO), has signed a Preferred Provider Agreement (PPA) with Aegerion Pharmaceuticals, a biopharmaceutical company focused on the development and commercialization of therapies for rare diseases. Veristat has assisted Aegerion with FDA, EU Market Authorization Application, and Japan Food and Drug Administration submission projects over the past 5 years.
Veristat will offer Aegerion clinical trial support including statistical consulting, biostatistical analysis, clinical data management, clinical monitoring, SAS programming, clinical protocol and study report writing, project management and the preparation of regulatory submission documents.
“Veristat has been a strong and dedicated collaborative partner and an extension of our project teams,” said Pamela Foulds, vice president of clinical development, Aegerion Pharmaceuticals.
“Veristat is thrilled to progress to this next phase in our working relationship with Aegerion,” said Barbara Balser, chief scientific officer, Veristat. “We feel like a true partner to Aegerion and are eager to continue to deliver quality expertise and services for their marketing applications.”
Veristat will offer Aegerion clinical trial support including statistical consulting, biostatistical analysis, clinical data management, clinical monitoring, SAS programming, clinical protocol and study report writing, project management and the preparation of regulatory submission documents.
“Veristat has been a strong and dedicated collaborative partner and an extension of our project teams,” said Pamela Foulds, vice president of clinical development, Aegerion Pharmaceuticals.
“Veristat is thrilled to progress to this next phase in our working relationship with Aegerion,” said Barbara Balser, chief scientific officer, Veristat. “We feel like a true partner to Aegerion and are eager to continue to deliver quality expertise and services for their marketing applications.”