--- description: ¿Qué piensan los usuarios de ValGenesis? Lee las reseñas y opiniones verificadas, descubre sus características y el nivel de usabilidad, consulta los precios y conoce las ventajas y desventajas de ValGenesis gracias a Capterra Panamá. image: https://gdm-localsites-assets-gfprod.imgix.net/images/capterra/og_logo-e5a8c001ed0bd1bb922639230fcea71a.png?auto=format%2Cenhance%2Ccompress title: ValGenesis - Opiniones, precios y características - Capterra Panamá 2026 --- Breadcrumb: [Inicio](/) > [Software para laboratorios de análisis clínicos](/directory/20043/medical-lab/software) > [ValGenesis](/software/127262/valgenesis) # ValGenesis Canonical: https://www.capterra.com.pa/software/127262/valgenesis > Un sistema de gestión de ciclo de vida de validación empresarial que gestiona un proceso completo de ciclo de vida de validación. > > Veredicto: 4 usuarios lo han valorado con **4.0/5**. De los mejores valorados en **Probabilidad de recomendación**. ----- ## Vista rápida ### ¿Quién usa ValGenesis? 1\. Empresas de ciencias de la vida 2. Fabricantes farmacéuticos y de medicamentos 3. Dispositivo médico 4. Biotecnología ## Estadísticas y valoraciones rápidas | Métrica | Calificación | Detalles | | **En general** | **4.0/5** | 4 Opiniones | | Facilidad de uso | 3.3/5 | Basado en las opiniones generales | | Asistencia al cliente | 4.5/5 | Basado en las opiniones generales | | Relación calidad-precio | 3.8/5 | Basado en las opiniones generales | | Funciones | 4.3/5 | Basado en las opiniones generales | | Porcentaje de recomendaciones | 80% | (8/10 Probabilidad de recomendación) | ## Sobre el proveedor - **Empresa**: ValGenesis - **Constitución**: 2005 ## Contexto comercial - **Precio inicial**: USD 12,000.00 - **Público objetivo**: 11-50, 51-200, 201-500, 501-1,000, 1,001-5,000, 5,001-10,000, 10,000+ - **Despliegue y plataformas**: Cloud, SaaS, Web, Mac (desktop), Windows (desktop), Windows (local), Android (móvil), iPhone (móvil), iPad (móvil) - **Idiomas admitidos**: inglés - **Países disponibles**: Alemania, Arabia Saudita, Argentina, Australia, Austria, Bangladés, Brasil, Bulgaria, Bélgica, Catar, China, Corea del Sur, Croacia, Dinamarca, Emiratos Árabes Unidos, España, Estados Unidos, Estonia, Filipinas, Finlandia y 32 más ## Funciones - Gestión de auditorías - Gestión de calibración - Integración de instrumentos de laboratorio ## Integraciones (en total: 1) - Jira ## Opciones de asistencia - E-mail/Help Desk - Preguntas frecuentes/foro - Base de conocimientos - Asistencia telefónica - Asistencia 24/7 - Chat ## Categoría - [Software para laboratorios de análisis clínicos](https://www.capterra.com.pa/directory/20043/medical-lab/software) ## Alternativas 1. [TELCOR RCM](https://www.capterra.com.pa/software/119399/telcor-rcm) — 4.7/5 (16 reviews) 2. [Avalon Laboratory System](https://www.capterra.com.pa/software/33053/avalon-laboratory-system) — 4.8/5 (16 reviews) 3. [MasterControl Quality Excellence](https://www.capterra.com.pa/software/148577/mastercontrol) — 4.5/5 (526 reviews) 4. [Document Control](https://www.capterra.com.pa/software/152366/document-control) — 4.4/5 (124 reviews) 5. [CGM LABDAQ](https://www.capterra.com.pa/software/120809/cgm-labdaq) — 4.3/5 (45 reviews) ## Opiniones ### "One of the best software systems used during the past 5 years" — 5.0/5 > **Usuario verificado** | *24 de mayo de 2018* | Productos farmacéuticos | Valoración de la recomendación: 10.0/10 > > **Puntos a favor**: Before using Valgenesis system, our validation process was paper based. We were creating about 300 - 400 validation documents per month, each document requires manual review, approval, then execution again review and approval. It requires about 4 - 6 weeks to complete a single document. After using Valgenesis system, everything was electronic including execution, exception management etc. we were able to complete the same document in a week time. All the bad hand writing issues were completely eliminated. We were challenged by QA all the time, after implementing Valgenesis in 2019, the observations went down by over 90%. > > **Puntos en contra**: In the old version, help file was not that great. It was improved in the current version. I was told that the next version to be released will have video help files throughout the application. > > Eliminated non compliance related issues. Reduce validation time by 70%. No preparation for audits. ----- ### "Paperless Validation Lifecycle Management" — 5.0/5 > **Muralikrishnan** | *26 de enero de 2022* | Dispositivos médicos | Valoración de la recomendación: 10.0/10 > > **Puntos a favor**: Strong functionality of end to end process starting from creating an inventory, entity, assessing the validation needs, creating system / requirement level assessment, requirements, traceabiliity matrix. Stronger test execution and capturing deviations. Well managed change request process > > **Puntos en contra**: There were some challenges on user interface which got significantly improved in the Version 4.0 > > Strengthening the compliance overall and the Regulatory team loved it ----- ### "One of the worst pieces of software I've ever seen" — 1.0/5 > **Usuario verificado** | *8 de marzo de 2018* | Valoración de la recomendación: 0.0/10 > > **Puntos a favor**: It makes me miss another tool that me and my team thought was bad (IBM Rational). In some sense, this is a pro. The animations of the workflow chart are a nice (hopeless) try. Has some certifications that make it compliant to highly regulated environments. > > **Puntos en contra**: We are forced to use it to track software change requests in a large enterprise. We asked for Jira, but incredibly this one has certifications that Jira hasn't. You're forced to use Internet Explorer (\!\!\!), and it opens the kind of popup - full screen, not resizable - where you don't get the urls. So no bookmarks. But it doesn't matter, you'd have to log in every time anyway and start from the beginning. If you happen to have a small screen, you're condemned to pain and tears, in a maze of scrollbars appearing everywhere. Searching for tickets is done through some reports that are for the most part readonly - that is, you can't click to see more details. From some you can though, but once you drill down, you might have to start from the beginning to check another ticket. Can't say anything about customer support (we're not in charge of configuration) but I guess it's not that great, since we asked to fix the incredible amount of notifications we get daily and nothing has changed in weeks. Yes, we really miss IBM Rational. ----- ### "Managing our validation program" — 5.0/5 > **Ram** | *26 de enero de 2022* | Biotecnología | Valoración de la recomendación: 10.0/10 > > **Puntos a favor**: The entire validation program is paperless through ValGenesis VLMS. We don't need to use any paper on the production floor. In the paper-based process, we spend weeks executing the validation protocols, then reviewing and approving through the manual process. Now it is 100% digital and takes only a few days and sometimes a few hours to complete the execution tasks. > > **Puntos en contra**: Nothing to dislike. Since the product is comprehensive and we are a small company, it requires some time to set up the system and training to use the system. We can't blame the system for this additional effort, most of the global companies are using ValGenesis as the system of records for their validation program, so naturally, the system is comprehensive. > > Great investment and effort to move our validation program into ValGenesis. We don't need to worry about any audits, in the past 2 years, there was no observation with our validation program. ## Enlaces - [Ver en Capterra](https://www.capterra.com.pa/software/127262/valgenesis) ## Esta página se encuentra disponible en los siguientes idiomas | Local | URL | | en | | | en-AE | | | en-AU | | | en-CA | | | en-GB | | | en-IE | | | en-IL | | | en-IN | | | en-NZ | | | en-SG | | | en-ZA | | | es | | | es-AR | | | es-CL | | | es-CO | | | es-CR | | | es-DO | | | es-EC | | | es-MX | | | es-PA | | | es-PE | | ----- ## Datos estructurados