




ClarityWriting
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Dr. Claire Fielden
Freelance medical and value communications writer
claire.fielden@claritywriting.co.uk
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Freelance medical writing services for the pharmaceutical and healthcare industries
Descriptions of writing services available
Market Access/
HEOR
A range of market access deliverables are available.
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New content development for core global and regional value dossiers, HTA submissions, value slide decks, AMCP dossiers, NICE, AWMSG, and SMC submissions, objection handlers, leave pieces. incorporation of health economics and outcomes research into value dossiers and slide decks, including RWE, SLR, meta-analyses, BIMs, cost-effectiveness analyses, patient-reported outcomes. Data-checking, creation of highlighted reference packs.
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Value
messaging
The development of value messages, influencing market positioning.
Strong value messaging for a competitive landscape. Identification of clinical, economic, and real-world evidence in support of value message development. Assessment of treatment and payer landscapes, and competition analysis, to assist clients with market access decisions. Insights into patient need extrapolated from patient reported outcomes and real-world evidence. Core value slide decks, payer-oriented value communications.
Medical communications
Dissemination of your medical and health-related information.
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New manuscript preparation and submission, with guidance through the whole manuscript submission process, from conception to publication. Preparation and submission of abstracts for congresses, poster design and preparation of congress presentation slide decks, including the script where required, to ensure that the presentation does not run over time.
Patient information/
lay summaries
Clear writing that patients and their families can understand.
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Clear information about medical conditions, treatments and procedures that patients and their families can understand. Preparation of lay abstracts to support scientific publications. Patient information booklets and leaflets to help patients understand a disease and its treatments.
Regulatory documents
Preparation of complex regulatory documents.
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Clinical Evaluation Reports, Clinical Study Reports, Post-Market Clinical Reports, Statistical Analysis Plans, Risk Evaluation and Mitigation Strategy, or other technical documents associated with clinical research to cover the entire drug and medical device development process.
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Other writing services
Copy development aimed at target audiences.
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Educational materials for medical or healthcare courses, articles for a newsletter or website, medical device product launch literature, opinion pieces. Proofreading, editing, literature searches, data checking, and rephrasing work written by non-native English speakers also available.
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