WHERE WE CAN HELP
With each phase of drug development come new deliverables and new challenges. Our experienced team are able to provide support and expertise throughout, advising on strategy and delivering high quality data analysis and documentation in addition to robust pharmacovigilance solutions.
Click on the phases below to find out more about where Effective Medical can help.
Phase 0-l
Phase ll
Phase lll
Phase lV
Experts
As the drive to create world-leading profitable drugs intensifies and the operating margin of drug development grows tighter, the reporting required by regulators can often be an unwelcome, albeit critical, overhead. Effective Medical helps pharmaceutical and research firms by providing regulatory and pharmacovigilance writing experts to assist with the reports, documentation and data analysis required as mandated by regulatory requirements.
About Us
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.
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Careers
Effective Medical is a growing business in a thriving industry. We’re always looking to hire great people with experience in medical regulatory, pharmacovigilance and general medical writing.
Contact us
To find out more about how Effective Medical can help you, please get in touch with us on +44 (0)845 0522420 or complete our contact form and we will be in touch as soon as possible.
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