Track recurring MoCRA work across products and facilities.
Marketplace evidence is easier to answer when the underlying records already have owners, dates, sources, and review controls. The Syntera MoCRA Compliance Evidence & Renewal Control System is built for businesses managing more than a single request: multiple products or facilities, recurring annual product-listing updates and biennial facility renewals, safety records, adverse-event intake, recalls, FDA records requests, and marketplace submissions.
The one-time Excel workbook carries forward the marketplace-evidence workflow concept from the $39 entry offer but adds the deeper registers, dashboard, and renewal structure needed for recurring work. There is no subscription. The dashboard and registers connect the company's roles, facilities, products, submissions, evidence, actions, and source scope.
The system helps a team see what exists, what is missing, who owns the next action, when a record was last verified, and what date or event should trigger review. It does not independently determine whether a company qualifies for an exemption, whether a product is a cosmetic or drug, whether an adverse event is serious or reportable, or whether a legal duty applies.
Syntera is an independent operational-aid provider and is not affiliated with or endorsed by FDA or TikTok. The system helps users organize and control their own records. It is not an FDA certificate, FDA verification, FDA approval, legal advice, a filing service, an automated regulatory decision-maker, or a guarantee of compliance or marketplace acceptance.





