PharmaVigilance serves the needs of various pharmaceutical companies as per regulatory requirements. We provide regulatory and medical writing services throughout the lifecycle of the product, from preclinical development to marketing authorisation and product maintenance phase. PharmaVigilance recognises that our clients require stable yet flexible solutions to manage fluctuations in volume, timelines and document types. We have managed a number of writing projects worldwide. Unlike many writing services that rely on freelancing contributors, PharmaVigilance employs a full-time staff of experienced medical writers who have extensive backgrounds in most therapeutic areas. Our medical writing specialists work closely with our colleagues in the PV, Regulatory Affairs, Quality Assurance and Publishing teams to deliver accurate and cost-effective projects to the highest ethical and scientific standards, within given timelines.