
Dossier Preparation
At RSA, we offer expert dossier preparation services designed to streamline the regulatory approval process. Our experienced team ensures that all necessary client documentation is compiled, reviewed, and submitted according to the specific requirements.
Our Dossier Preparation Services
Data gap analysis
RSA can review data for technical completeness against the data requirements detailed in Commission Regulations (EU) No 283/2013 and 284/2013, associated guidance documents, relevant scientific opinions and any vulnerability to classification under the CLP Regulation ((EU) No 1272/2008). Any findings of concern can be highlighted as well as the need for additional toxicology studies, where relevant, and a testing strategy can be recommended.
Risk Assessment
RSA specialists are experienced in performing both human health and environmental assessments. With a broad range of toxicological, testing and regulatory expertise, as well as experience with alternative methods (in vitro, in silico, QSAR and read-across) and literature searching, our experts can offer guidance on the hazard and risk of chemicals.
Study Summaries (OECD and IUCLID)
Preparation of summaries, both of study reports and literature papers, is a crucial part of dossier preparation. RSA can help prepare OECD, OHT, IUCLID and DER summaries. All summaries are peer reviewed for quality and consistency ready for inclusion in submission documents.
CRO Liaison
From selecting the right CRO, designing a robust study plan, through to data interpretation and reporting, the RSA study monitoring team have the experience necessary to advise on any issue, ensuring that our clients are kept informed and have confidence that their studies are being monitored to the highest standards.
Literature Searches
RSA is experienced in performing and documenting systematic literature searches according to EFSA Guidance, including assessment of published literature for relevance and reliability.
Dossier Preparation Specialists

Our Team
RSA's world-class consultants are committed to providing you with the support that will address and resolve complex issues and achieve regulatory compliance.
Our Team >
Sectors we work with
Blog

Unveiling the indirect liver enzyme mediated thyroid effects of Valifenalate on rats and dogs which is not relevant to humans

Framework for classifying chemicals for repeat dose toxicity using NAMs
