Federal Register Notice: FDA is making available draft guidance for industry: Providing Regulatory Submissions in Electronic Format — Receipt Date. It provides information on what the agency will consider to be the receipt date for certain submissions provided in electronic format to CDER and CBER. FDA will not consider a submission to be received until it has passed a technical validation check to ensure that the submission can be opened, processed, and archived. To download this guidance, click here. To view this notice, click here.