Flexible, reliable and fast-paced
PHARA+ people serve the client by assisting the company’s regulatory affairs department in hands-on execution of company defined regulatory strategies and plans through sharing their scientific background, regulatory knowledge and communication skills.
They submit applications, run procedures, liaise with authorities and company internal stakeholders.
They can be called upon when to complement existing resource, act as interim staff or provide additional manpower to cope with workload peaks or special projects.
Regulatory tasks our people can support include clinical trial applications and marketing authorisation life cycle management and pre-authorisation support via EU CP/MRP/DCP and national BENELUX procedures.
PHARA+ aims to develop long standing sustainable partnerships with its clients by sharing its regulatory talent.