Pearl IRB has created a reputation of quality medical writing for companies of all sizes, from global powerhouses to small startup clients. Our employees have decades of experience in facets such as:
- Design and authoring of protocols and informed consent forms
- writing publications including posters, speaker PowerPoint decks, and articles
- creating regulatory documents, clinical trial summary report, CER (Clinical Evaluation Report), and for peer reviewed journals
- providing other detailed clinical trial forms and documents
Our IRB is determined to solve your problems. Whether a client needs help in creation of the original documents, editing, or just a second set of eyes on critical documents, we can help. We also have a biostatistician on staff who partners with our medical writers when statistical powering calculations or statistical analysis is needed. Through our expertise and experience, Pearl IRB has the ability bring you through the submission process.