array(9) { ["sf_event_start_date"]=> array(1) { [0]=> string(12) "May 17, 2022" } ["sf_event_end_date"]=> array(1) { [0]=> string(12) "May 17, 2022" } ["sf_event_description"]=> array(1) { [0]=> string(972) "FDA requirements are changing for medical device manufacturers. Your business risks losing contracts by ignoring these new regulations. Furthermore, these updated rules could lead to mandatory product recalls. Enroll in the Harmonizing Current Good Manufacturing Practices (cGMP) with ISO 13485 to learn how to avoid these costly penalties and stay up to date with the new rules and requirements.

Following cGMP is no longer enough for medical device manufacturers. Manufacturers that follow cGMP must now align themselves with ISO 13485 standards under the new requirements. This course will update manufacturers on the most recent changes to the regulations so ‘MADE in New Jersey’ businesses don’t lose out on any critical contracts and avoid any costly audits. By attending this online course, you’ll find out how to merge your cGMP with ISO 13485 standards to ensure your facility is in good standing.

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