TrialSummaries.com: By the Numbers

8 Tips for Producing Masterful Plain Language Summaries

To ensure you craft high-quality plain language summaries that meet European Union regulatory requirements, follow these best practices.

Citeline Expands Biotech’s Bandwidth with Regulatory & Medical Writing Services

In this case study, Citeline expands the bandwidth, expertise, and resources of a mid-size biotech to help handle its regulatory writing requirements.

Get the Answers You Need Faster – A Guide to Citeline Regulatory Solutions

Clinical trial disclosure can be a heavy burden for biopharma. This guide provides an overview of how Citeline helps throughout the regulatory process.