medical writing services
NEA medical writing services range from nonclinical manuscripts, to regulatory submissions and clinical documents, to copywriting for the trials and marketing of your next drug, to continued medical education of medical professionals.
Our team of uniquely qualified experienced medical writers can provide you quality, timely, affordable technical documents. Our Medical Writers are excellent scientific communicators and seasoned scientists. They each have an advance degree such as PhD, MPH, RNs and possess an average of 15 years of scientific writing experience. Many of us have several published papers in leading bioscience journals to our own credentials. We know how to write accurate and concise scientific documents for technical audiences as well as understandable and engaging medical documents for the general public.
NEA offers full-service assistance, from preclinical phases to commercialization and beyond. By collaborating with our team – that is as skilled in the nitty-gritty details and infrastructure of early development as it is with late-phase trials, regulatory requirements, and market access – you can get a robust customized content and strategic roadmap to get you where you want to go. Our team has been working with leading CME companies, biotech companies, academia and regulators. Based upon their encouraging feedback, we are starting Medical Writing as a practice.
medical writing expertise tailored to your project
Knowing how to navigate the medical, regulatory and legal review process is quintessential to getting your message across. NEA medical writers create custom content that connects all the points while ensuing to present it in the optimal way to streamline the approval processes and reduce the amount of revisions.
NEA have developed proprietary processes to maximize the time and communication we have with our clients and review teams. It’s our ability to package content submissions for streamlined client reviews, complete regulatory submissions and beyond, at all stages in the product lifecycle that makes us an invaluable medical writing partner.
how we help
NEA medical writing team brings experience, attention to detail, and robust quality control processes to work for your clinical trials and associated scientific fields. Our in-house medical writing team understands the science behind your study and adds an extra layer of experienced data review and messaging that create higher value for all stakeholders.
With a diverse team of medical science professionals, we can cover just about any therapeutic and biomedical area. By now, we are all good at researching and learning new areas as well. Our body of work includes:
- Bioinformatics
- Basic science: Biochemistry, structural biology, molecular biology, drug design, chemistry, computational biology, anatomy, others!
- Cardiology / Cardiovascular medicine
- Diabetes / Metabolic syndrome
- Genomics
- GI (Gastrointestinal) and digestive biology
- Kidney disease
- Neuroscience
- Oncology
- Psychiatry / Mental Health / Psychology
- Rheumatology
- Toxicology
- Wound Healing
We have helped major CME companies like WebMD, smaller biotech companies, medical centers and research centers. No project is too big or too small. We work remotely and serve clients across USA and around the world.
Please reach out to us. We are happy to discuss your needs and provide a quote.
– Medical Writing Director
North End Advisory
Email: MedWriting@NEAdvisory.com
what we think
medical writing experts on demand
Whether it’s a first clinical protocol, a pivotal trial protocol, or associated documents such as the ICF, the investigator’s brochure, or a full IND/IDE, NEA brings the therapeutic, clinical, regulatory, and medical writing expertise needed to ensure quality documentation for the success of your next project.
Got a Project or
Partnership in Mind?