Medical Writing Services, Regulatory, Clinical, Medical Writing

Medical Writing is a vital segment of clinical research. It plays a critical role in the development and submission of clinical research documents and defines the success or failure of new medicinal products/devices. As Regulatory authorities expect precise and timely submissions of documents/dossier, any delay in this stage leads directly to a delay in realizing profits both in terms of achieving patient benefit and ROI.

With a qualified (Medical and Paramedical) team of skilled and experienced medical writing professionals from pharmaceutical and clinical research industries,, Freyr develops quality documents, performs peer review and coordinates client reviews, performs the quality checks, and accomplishes the project management of various Regulatory, clinical and medical writing activities. The Freyr medical writing team, with a proven proficiency in developing and delivering world-class Regulatory and medical writing services for its growing clientele of (global large) Pharma, leading CROs and other Biotech companies adheres to stringent timelines and high-quality parameters.

Freyr is a preferred global medical writing services provider for writing, performing independent quality review and identifying gaps/performing gap analysis in already prepared/compiled dossier.