NMR MedComms help medical affairs and marketing teams with medical content that drives results and meets expectations.Industries we serve: Pharmaceuticals, Biotechnology, Clinical Research, Healthcare, and DiagnosticsOur main services (Medical Writing+Graphic Design Support): - Scientific Slide Decks | E-learning Module Decks - Infographics | Visual Summaries | Leaflets | Brochures| Factsheets- Articles| Blogs | Guides | Listicles | E-books | White Papers

Worked on a variety of medical writing deliverables for global pharma companies with proven experience working with medical communication agencies/PR agencies.My services include1. Scientific PowerPoint presentations2. Medico-marketing material3. Medical Copywriting4. Articles and reports covering topics related to Pharma, Biotech, Healthcare and Clinical Research industriesTherapeutic areas covered• Rare disease• Diabetes• Oncology• Cardiology• Women's health• Anti-infectivesCore Strengths• Ability to distil complex scientific data into articulate and engaging content (powerpoint decks, brochures, visual aids, e-detail aids, leave behind pieces, scientific articles, blog posts, storyboard)• Create content with clear, coherent presentation of data and key messages• Faultless attention to detail and ability to create content for a range of audiences • Proficient in conducting literature searches• Knowledge of major advancements in Pharma industry, key therapeutic areas and basic statistical concepts

Involved in developing engaging articles and listicles covering innovations in pharma, biotech and laboratory diagnostics.You can see a list of my published work in the link below:https://www.technologynetworks.com/tn/editor/neeta-ratanghayra-mpharm

Involved in developing engaging articles covering developments in pharma and laboratory diagnostics.You can see a list of my published work in the link below:https://www.clinicallabmanager.com/author/neeta-ratanghayra-m-pharm

Involved in developing engaging articles covering innovations in pharma and biotech.You can see a list of my published work in the link below:https://www.pharmasources.com/news/list/list-3-show-54.html

 Worked for clinical study projects (bioavailability / bioequivalence studies) given by different sponsors for submission to various health regulatory agencies like EMA, USFDA, TGA, WHO and Health Canada.• Performed quality checks in different in-process activities like screening, ICF presentation, check-in, dosing, vital examination, checkout, post-study and ensured that the study is conducted as per protocol, regulatory guidelines, International Conference on Harmonisation-Good Clinical Practice (ICH-GCP) and Standard operating procedures.• Retrospective quality checking of study documents like Informed consent form, screening case report form and study case report forms to ensure compliance with protocol, regulatory guidelines, International Conference on Harmonisation-Good Clinical Practice(ICH-GCP) and Standard operating procedures.• Report the observations found during in-process audit and retrospective audit of documents in writing to the concerned department/person. To verify responses given for the query generated.• To maintain all QC reports in file and archive them. To request and maintain accountability of all study related documents.• Preparing study for Quality assurance audits, sponsor audits and regulatory audits.• To conduct study initiation meeting. To provide SOP training to other staff as and when required.• To help in clinical study report preparation

 Worked for clinical study projects (bioavailability / bioequivalence studies) given by different sponsors for submission to various health regulatory agencies like EMA, USFDA, MHRA, TGA, WHO and Health Canada.• Development of study specific monitoring plan. Online monitoring of clinical study to ensure sponsor obligations are met and are compliant with protocol, regulatory guidelines, International Conference on Harmonisation-Good Clinical Practice (ICH-GCP) and Standard operating procedures.• Retrospective review of clinical study raw data to ensure accuracy, completeness and compliance with protocol, regulatory guidelines, International Conference on Harmonisation-Good Clinical Practice (ICH-GCP) and Standard operating procedures. Raw data included medical screening records, informed consent forms and case report forms.• Review of clinical study report as per raw data, International Conference on Harmonisation-E3 (ICH E3), protocol, regulatory guidelines and sponsor specifications.• Inspecting clinical study related training to check compliance to study protocol.• Preparing study for Quality assurance audits, sponsor audits and regulatory audits.• Issuance of various documents (Medical Screening records, Informed consent forms, Case report forms etc.), with controlled copy number, required for conducting clinical study.• Preparation of study for archiving after study completion.