I started MOR Medical Writing in April 2020, with more than 20 years’ experience behind me. The company provides scientific and medical writing services to the pharmaceutical industry, CROs, academia, consultants and corporate clients.
My experience covers early and late stage clinical development and due diligence activities, which collectively has involved multiple encounters with regulatory authorities and scientific advice, bringing knowledge and insight to a diverse range of projects and therapeutic areas.
Therapeutic areas covered up to 2020 have included Vaccines against infectious disease agents, Neurology, Haemophilia, Biotherapeutics, Biosurgery, Aesthetics, Opthalmology and Orthopaedics (for medical products and devices).
Since April 2020 I have written several regulatory submission documents for a variety of clients, comprising clinical study protocols, clinical study reports, DSURs, paediatric investigation plans (and iPSPs), clinical overview & clinical summary updates, clinical evaluation plans, clinical evaluation reports, reports of prior investigations, summaries of safety and clinical performance and publications. The therapeutic areas covered include Cardiology, Oncology, Rare Diseases, Neurology, Dermatology, Opthalmology, Orthopaedics, and Vaccines (prophylactic and therapeutic).
The services offered are tailored to meet your needs and budget, whether that is writing your document, providing assistance, or performing a final, review, QC, language check and format of your document (Pricing/Strategy). I have a strong background in preclinical and clinical R & D and substantial experience in the preparation of regulatory submission documents, reports and publications across a diverse range of therapeutic areas, sufficient to meet your project needs (CV link, LinkedIn). I love what I do, I enjoy challenges and I look forward to assisting you with your scientific or medical writing needs.
