Preclinical study reports
Writing, reviewing, and editing of preclinical reports is often a rate-limiting step for pharmaceutical companies. Outsourcing to Pharma Consulting Aachen allows efficient and impartial processing of this task in one hand. Our services cover preparation and evaluation of pharmacological, toxicological, and pharmacokinetic expert reports, as well as documents on pharmaceutical quality.
We provide and evaluate independent expert reports to clarify factual situations in legal conflicts. These can involve clinical, pharmacological, toxicological, pharmacokinetic, and biochemical issues.
Environmental risk assessment (ERA) reports
A guideline on the environmental risk assessment of medical products for human use has been implemented since December 2006. Pharma Consulting Aachen supports companies dealing with this requirement by reviewing study designs, analysing data and writing the corresponding reports.