Electronic Submissions (eCRT)

TechnoSTAT's experienced staff will accurately compile and prepare your electronic data submission, bringing it in line with FDA requirements. We make use of our extensive experience in SAS software to develop regulatory compliant tabulation of case report forms (CRFs) and data definition tables. When preparing eCRT submissions, TechnoSTAT will:

• Customize its solution to company needs, taking into account FDA review
• Produce eSUB deliverables
• Integrate and standardize relevant data from, if necessary, differences sources and in different formats