Available In Different Color Preparation Of Sops

Trial specific regulatory/compliance and clinical advice and strategy at
the early stages of product development can be critical to the ultimate
approval of the product. Failure to address regulatory and compliance
concerns early in the development program often results in delays in
approval due to improperly designed studies, omitted studies,
manufacturing oversights and other failures to meet key regulatory
requirements. Timely submission of all trial related documents,
including proper Standard Operating Procedures, could play a crucial
part in the sponsors decision to accept the site for specific trials.
Academy of Clinical Research professionals are highly versed in
generating site specific SOPs, and proper completion and submission of
all required regulatory file documents and logs.