Ya­veon 365 dig­i­tal­ly doc­u­ments ev­ery batch.

From ware­house re­ceiv­ing to ship­ment, the so­lu­tion au­to­mat­i­cal­ly re­cords ev­ery move­ment and change.

E­lec­tron­ic batch re­cords (eMBRs), au­dit trails, and re­lease pro­to­cols en­sure com­plete doc­u­men­ta­tion.

The ERP au­to­mat­i­cal­ly gen­er­ates re­call re­ports.

Ya­veon 365 cen­tral­ly main­tains for­mu­la­tions, in­clud­ing pre­cise ac­tive in­gre­di­ent and nu­tri­tion­al val­ue cal­cu­la­tions.

Chang­es or new ver­sions are con­trolled dur­ing ap­prov­al, while la­bels au­to­mat­i­cal­ly a­dopt the cur­rent dec­la­ra­tion da­ta.

Ya­veon 365 sup­ports GMP-com­pli­ant work through e­lec­tron­ic in­spec­tion plans, dig­i­tal sig­na­tures, and trace­a­ble ap­prov­als.

The so­lu­tion sys­tem­at­i­cal­ly i­den­ti­fies and as­sess­es de­vi­a­tions or OOS cas­es (out of spec­i­fi­ca­tion) and doc­u­ments them via CA­PA work­flows.

Wheth­er pri­vate la­bel or own brand: our in­dus­try-spe­cif­ic ERP maps mul­ti-lev­el pro­duc­tion pro­cess­es, in­clud­ing cus­tom­er-spe­cif­ic rec­i­pe pack­ag­es and doc­u­ments.

Var­i­ants and ap­prov­als re­main clear­ly sep­a­rat­ed and are trace­a­ble at all times.

The ERP au­to­mat­i­cal­ly match­es cer­tif­i­cates of a­nal­y­sis (COAs) with the stored spec­i­fi­ca­tions.

Au­dit re­sults, in­spec­tion re­ports, and cer­tif­i­cates are in­clud­ed in the sup­pli­er e­val­u­a­tion and de­ter­mine the re­spec­tive ap­prov­al sta­tus.

Sta­bil­i­ty da­ta and shelf-life rules au­to­mat­i­cal­ly gov­ern dis­po­si­tion and re­lease pro­cess­es.

A batch is on­ly re­leased once all in­spec­tions are com­plete and the doc­u­men­ta­tion cri­te­ri­a are ful­ly met—com­plete­ly dig­i­tal and au­dit-proof.