Effective Medical is a full service agency with expertise in all aspects of pharmacovigilance and regulatory writing services. We can assist throughout Phases I-IV of the drug development lifecycle and work both directly with pharmaceutical/biopharmaceutical firms and indirectly partnering alongside major Clinical Research Organisations (CRO’s). We provide a flexible approach and can tailor all services to suit individual needs. As a privately owned organisation, we are able to modify our operating approach to suit a customer’s specific requirements. With some customer and partner engagements, we are used as an ‘overflow’; making services available at short notice when required to assist in meeting very tight deadlines with complex drug submissions. Other customers and partners prefer to outsource entire programmes or work to us. We will flex to suit your needs. Our approach and philosophy can be summed up in three words: quality, speed and flexibility. Our customers and partners are often operating under restricted time conditions, often with a complex data landscape and have no time for multiple reviews, re-submissions and quality assurance checkpoints. Simply stated, output needs to be right, first time and completed to the highest standards. At Effective Medical, we employ only the highest quality of staff and have structured our company with both quality and speed of delivery at our core. All writing staff are experienced pharma or medical professionals previously holding positions at pharmaceuticals or CRO’s. Effective Medical never uses low-cost or offshore regions.