Scientific & Regulatory Documentation

Clinical trials require the writing of a wide range of documents for regulators and scientific journals. These must be accurate and detailed, which can take time and resources.

We provide a comprehensive range of high-quality writing solutions to help clients accurately and authoritatively present their trial’s findings. We understand the complexities involved in writing investigator’s brochures and will update text in-line with available data to ensure clarity for investigators and regulatory agencies.

Our experts are drawn from multidisciplinary backgrounds and have advanced degrees and experience in multiple therapeutic areas. They understand your requirements, the needs of your audience and will get the best out of complex clinical trial data. All information is presented in line with current regulations, ensuring compliance and clarity.

Our specialists support the writing of a wide range of documents, including:

• Investigator’s brochures
• Clinical trial summaries
• Scientific articles
• Literature reviews

SGS is recognized as the benchmark for quality and integrity in medical writing services. Whatever your requirements, our experts ensure data is presented clearly and in compliance with regulatory requirements to expedite access to market.