EXPERIENCED WRITERS WITH A MEDICAL BACKGROUND

All of our writers are qualified to an MsC, PhD or MD level and have at least 6 years of professional experience writing and editing medical documents.

ENSURED SECURITY AND CONFIDENTIALITY

Your sensitive and confidential documents are safe with us. We use secure file systems, and all of our experts work under a binding NDA.

SUBJECT MATTER EXPERTS FOR EACH WRITING PROJECT

For each writing project, we carefully select the best match from our extensive global network of writers, based on subject matter and client requirements.

Medical Writing Solutions

We deliver accurate writing services, in a timely and confidential manner

When your medical document needs to click all of the right boxes—scientifically accurate, clear, culturally sensitive, fully compliant with current regulations, adapted to the target audience—we’ll find the right medical writer for you in the Novalins network.

That’s because our geographically and professionally broad team includes more than 600 medical writers located in 100 countries.

Writers are qualified to the MSc or PhD level, and they possess full knowledge of industry guidelines and vast experience in writing and editing medical documentation. They’re also trained in a wide range of therapeutic fields including Biochemistry, Cardiology, Diabetes, Endocrinology, Neurology, Oncology, Rheumatology, and Toxicology.

Writers undergo regular training conducted by the EMWA (European Medical Writers Association), the AMWA (American Medical Writers Association) and other recognized medical writing organisations to keep their skills at the vanguard of the medical-writing field.

 

This vast and diverse network of expert medical writers offers the following key benefits for your project:

  1. As many writers as necessary can work on it to complete it in the timeframe you need. Practically no deadline is too tight.
  2. It will be culturally sensitive to the locale you wish to operate in.
  3. Pricing remains competitive.Our medical writing services are fully compliant with ICH Guidelines and other regulatory requirements currently in force. We strictly follow our internal SOPs or apply our client’s specific SOPs, templates, and writing style for a wide variety of documents, including Regulatory, Clinical, and Medical communication materials such as:
  • Clinical Study Reports (CSRs)
  • Study Protocols
  • Clinical and non-clinical sections of Common Technical Documents (CTDs)
  • Clinical sections of New Drug Applications (NDAs)
  • Pharmacovigilance documents
  • Investigator Brochures
  • Patient information (Informed Consent Forms, Patient Brochures)
  • Standard Operating Procedures (SOPs)

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