Paraphrase the paragraph:
The IMPD shall provide a critical analysis of the data, including justification for omissions of data, and an assessment of the safety of the product in the context of the proposed clinical trial rather than a mere factual summary of the studies conducted.
IMP documentation, instead of a mere factual summaries of studies performed, provides a critical data analysis, including rationale for omission of data, as well as a product Safety Assessment, related to a proposed clinical trial.