{"id":19,"date":"2019-01-08T17:31:31","date_gmt":"2019-01-08T17:31:31","guid":{"rendered":"http:\/\/phara.eu\/paraplus\/?page_id=19"},"modified":"2019-07-09T08:44:34","modified_gmt":"2019-07-09T08:44:34","slug":"services","status":"publish","type":"page","link":"https:\/\/phara-plus.be\/pharaplus\/services\/","title":{"rendered":"Our services+"},"content":{"rendered":"<p class=\"subheader\">Flexible, reliable and fast-paced<\/p>\n<p>PHARA+ people serve the client by assisting the company\u2019s regulatory affairs department in hands-on execution of company defined regulatory strategies and plans through sharing their scientific background, regulatory knowledge and communication skills.<\/p>\n<p>They submit applications, run procedures, liaise with authorities and company internal stakeholders.<\/p>\n<p>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.<\/p>\n<p>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.<\/p>\n<p>PHARA+ aims to develop long standing sustainable partnerships with its clients by sharing its regulatory talent.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Flexible, reliable and fast-paced PHARA+ people serve the client by assisting the company\u2019s regulatory affairs department in hands-on execution of company defined regulatory strategies and plans through sharing their scientific background, regulatory knowledge and communication skills. 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