Loftware Cloud Clinical Trials

    Loftware Cloud Clinical Trials (previously Loftware Prisym 360) streamlines clinical supplies labeling and content management – it’s built into our software’s DNA. Our solution removes costly unknowns by simplifying complexities and shortening timelines to deliver GxP-compliant labeling with consistency, accuracy, and speed.

     

    Keep your clinical supply labeling running smoothly – It’s all right there™

    Dokazana rešitev za označevanje v kliničnih študijah

    Omogočite doseganje skladnosti s standardi

    Poenostavite pregledovanje in odobritev etiket. Informacije, ki spremljajo klinične študije, so ključne za zagotavljanje varne in učinkovite uporabe. Poenostavljena rešitev vam pomaga enostavneje načrtovati in oblikovati vsebino etiket, vložkov in embalaže.

    Izboljšani odzivni časi

    Omogočite nove modele v dobavni verigi. Stroški presežkov zalog v kliničnih študijah in tveganje, da so klinična pakiranja napačno označena z zastarelimi podatki o izteku roka uporabnosti in odmerkih, so postali zelo pomembni dejavniki. Dinamično ustvarjanje etiket ponuja učinkovitost, hitrost in agilnost za omogočanje modelov tiskanja in izdelave embalaže na zahtevo.

    Poenostavite oblikovanje etiket in knjižic

    Keey running smoothly by moving beyond manual processes. Each country has their own regulatory and language requirements, however, you can automate processes to reduce clinical label and booklet design and printing from weeks to hours, while ensuring regulatory requirements are met and removing errors.

    Spodbujajte nenehne izboljšave

    Make connections by integrating with critical systems such as Clinical Supply Management (CSM), Enterprise Resource Planning (ERP), Product Lifecycle Management (PLM), and other data repository systems to retrieve the most up-to-date label data at the point of printing, providing accuracy and consistency.

    Centralizirajte nadzor za sledljivost

    Skip the worries by having full visibility. Maintain complete integrity of your label data to meet compliance with FDA & EU regulations, specifically FDA 21 CFR Parts 11, 810, and 820. Enabling a view of master data assets provides the ability to control, optimize and help ensure compliance.

    Podpora globalnim zahtevam

    Manage the complexity and avoid risk of error. As the number of countries included in each study increases, so does the need to meet specific regulatory content, phrase, and language requirements. Having an automated solution helps to reduce timescales and prevent errors.

    Rešitev za označevanje, ki omogoči učinkovite klinične študije

    Programska oprema Loftware Cloud Clinical Trials je poenostavila skladno označevanje na področju kliničnih študij. Etiketa ni zgolj besedilo in slike, ampak se pod njo skriva kompleksna struktura vsebine in podatkov. Od spremenljivega besedila do specifičnih zahtev za določene države in skladnosti s predpisi, prav vsaka podrobnost nekaj šteje.

     

    But at Loftware, we pride ourselves on knowing these intricacies in product identification. That’s our business. To provide you with a validation ready cloud-based labeling solution that’s simple, agile, and scalable. We enable you to remove costly unknowns by getting trials to market quicker and more cost effectively, allowing you to do what you do best… delivering patients a safe, positive, and effective trial outcome.​​

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    Connect with our specialists to explore Loftware Cloud Clinical Trials.

    It’s all right there with Loftware Cloud Clinical Trials

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