---
description: Tudo sobre TrialKit: preço, alternativas, vantagens e desvantagens, funcionalidades e avaliações de outros usuários. Saiba mais!
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title: TrialKit - Preço, avaliações e classificação - Capterra Brasil 2026
---

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# TrialKit

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> Clinical Studio facilita a pesquisa, fornecendo infraestrutura corporativa sob demanda, por uma taxa fixa.
> 
> Conclusão: 34 usuários atribuíram a nota **4.5/5**. Melhor classificado para **Probabilidade de recomendação**.

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## Resumo

### Quem usa o TrialKit?

Atualmente, Clinical Studio é usado por empresas farmacêuticas, de biotecnologia e de dispositivos, pesquisadores independentes e acadêmicos e por CROs, para realizar mais de 1.000 testes pré-clínicos e de fase 0 a IV em todo o mundo.

## Estatísticas e notas

| Métrica | Classificação | Detalhes |
| **Geral** | **4.5/5** | 34 Avaliações |
| Praticidade | 4.4/5 | Com base em avaliações gerais |
| Suporte ao cliente | 4.8/5 | Com base em avaliações gerais |
| Relação qualidade/preço | 4.6/5 | Com base em avaliações gerais |
| Recursos | 4.2/5 | Com base em avaliações gerais |
| Porcentagem de recomendação | 80% | (8/10 Probabilidade de recomendação) |

## Sobre o fornecedor

- **Empresa**: Crucial Data Solutions
- **Localização**: Reno, EUA
- **Fundada**: 2010

## Contexto comercial

- **Público-alvo**: 2–10, 11–50, 51–200, 201–500, 501–1.000, 1.001–5.000, 5.001–10.000, 10.000+
- **Implantação e plataformas**: Nuvem, SaaS, baseado na web, Mac (desktop), Chromebook (desktop), Android (celular), iPhone (celular), iPad (tablet)
- **Idiomas**: alemão, chinês, espanhol, francês, grego, holandês, inglês, italiano, japonês, norueguês, polonês, russo, sueco, tcheco, ucraniano
- **Países disponíveis**: Alemanha, Austrália, Brasil, Canadá, China, Estados Unidos, Japão, México, Índia

## Recursos

- Agendamento
- Captura de dados eletrônicos
- Captura distribuída
- Captura remota de dados
- Classificação de documentos
- Conformidade com HIPAA
- Conformidade com a Lei 21 CFR, Seção 11
- Design de teste
- Digitalização de documentos
- Gerenciamento de documentos
- Gestão de conformidade
- Gestão de estoques
- Gestão de formulários
- Gestão de pacientes
- Gestão do fluxo de trabalho
- Gestão financeira
- História clínica eletrônica/informatizada
- Importação/exportação de dados
- Monitoramento de pacientes
- Recrutamento de pacientes
- Registro de auditoria
- Relatórios e análise de dados
- Third-Party Integrations

## Opções de suporte

- Email/Help Desk
- Base de conhecimento
- Suporte por telefone

## Category

- [Software de Gestão de Testes Clínicos](https://www.capterra.com.br/directory/10035/clinical-trial-management/software)

## Categorias relacionadas

- [Software de Gestão de Testes Clínicos](https://www.capterra.com.br/directory/10035/clinical-trial-management/software)
- [Software de Captura de Dados Eletrônicos](https://www.capterra.com.br/directory/30551/electronic-data-capture/software)

## Alternativas

1. [Castor EDC](https://www.capterra.com.br/software/143532/castor-edc) — 4.7/5 (204 reviews)
2. [Viedoc](https://www.capterra.com.br/software/160680/viedoc) — 4.4/5 (95 reviews)
3. [Jotform](https://www.capterra.com.br/software/158456/jotform-4-0) — 4.7/5 (2813 reviews)
4. [ShareCRF](https://www.capterra.com.br/software/1031214/sharecrf) — 4.8/5 (44 reviews)
5. [ClinCapture](https://www.capterra.com.br/software/133931/clincapture) — 4.9/5 (21 reviews)

## Avaliações

### "Rapid Turnaround Time and Phenomenal Customer Service" — 5.0/5

> **Margaret** | *25 de junho de 2021* | Indústria farmacêutica | Taxa de recomendação: 10.0/10
> 
> **Vantagens**: It's not required that you hire a programmer to design and implement eCRFs with this system.  The training and customer service team is so incredibly helpful.  I was able to turn around an entire study's EDC setup within 3 weeks of getting contracts signed.
> 
> **Desvantagens**: Each time I've identified a pain point or a feature that I would like or wanted to work better, it was updated in the next release.  I don't currently have any unmet needs.

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### "TrialKit - Leadership that is transforming the biotechnology industry" — 5.0/5

> **Stephen** | *5 de fevereiro de 2022* | Biotecnologia | Taxa de recomendação: 10.0/10
> 
> **Vantagens**: Answered in previous section with regards to system performance
> 
> **Desvantagens**: The only improvement I would recommend is the add the capability to schedule jobs to automatically generate reports and send them to a sFTP.
> 
> Wonderful\!  I know that sounds short, but it really has been a system that I have grown to appreciate and enjoy working within.  The tech support and staff at TrialKIt are also a primary reason for my choice to go with TrialKit.   Working with TrialKit allows the versatility to have a solution for my clients where I can contour the system to meet their needs.

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### "No SLA, Accountability: Rolling out Validated Features that are not FDA Compliant" — 1.0/5

> **Grace** | *21 de julho de 2025* | Hospitais e Saúde | Taxa de recomendação: 0.0/10
> 
> **Vantagens**: Really disappointing software and software support. Sometimes we wait more than a week for a response and when FDA trial participants are not able to save their responses we lose 12-14 in a week at a time and do not recoup those costs.
> 
> **Desvantagens**: No accountability, very buggy software, not accountable for mobile-views of their surveying tools, audio fails during sessions, heavy push for additional mobile app development and delay after delay in fixes.&#10;&#10;Very costly, not knowing what features are validated for trials, allowing us to believe that certain features like mobile-view are validated--however, this was not true and more than 50% trial participant failures in this mode requiring us early on to purchase additional development for a mobile app separately because the mobile view was not actually validated. This was not communicated from the get-go and the trial delays and costs are unbelievable.&#10;&#10;There are trial costs and damages in the millions in working with Trial Kit and Fuel. No accountability and dangerous practices that should raise issues with any accreditations.
> 
> Shockingly poor, oversold, and once you're using, you cannot switch out during the trial. Misled by former reviews that were suspiciously high for a very buggy, unreliable product with poor service to boot.

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### "Medical Device Start-up Experience with TrialKit" — 5.0/5

> **Mindy** | *16 de dezembro de 2024* | Aparelhos médicos | Taxa de recomendação: 9.0/10
> 
> **Vantagens**: The team at Crucial Data Solutions had great customer service. They were promptly and consistently available to provide direct support during our build and throughout the study.
> 
> **Desvantagens**: I used TrialKit before TrialKit AI became available. At the time, some of the reporting functionality was cumbersome, making it more difficult to capture key performance metrics for our trial. I look forward to trying the AI tools as we plan for our next study.
> 
> Wonderful\! I would gladly recommend it to colleagues.

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### "Crucial Clinical Study Database review" — 4.0/5

> **Sarah** | *18 de junho de 2020* | Aparelhos médicos | Taxa de recomendação: 8.0/10
> 
> **Vantagens**: The process of working with the Crucial team was and continues to be seamless.  It was easy to obtain/access the software.  Our database developers used the software to create a database for a large, global clinical registry and the Crucial team has been very supportive of both the initial set-up as well as multiple updates to the database that have occurred along the way.  We have been able to integrate the platform easily within our clinical processes and customer service has been exceptional.
> 
> **Desvantagens**: Future development opportunities exist around reporting and metric-tracking.  Specifically, improving capabilities for clinical trial metrics and auto-generated reports.  Much of the current reporting requires that a user first exports the data followed by analysis and report generation through additional tools such as excel.  While this is technically functional, it would be fantastic to have more common reports available in the software that would allow you to view key information within your data at the click of your mouse.   For example, additional standard/customizable reports that contain aggregate data, summary information from your data, some data sorting capabilities, and tracking of metrics commonly used within a clinical trial stetting (e.g., monitoring metrics such as query aging, etc.) would make it even easier and faster to oversee any given clinical study.
> 
> Our business needed a cost-effective, easy-to-use solution that could support data capture for a complex, large-scale, global, medical device registry.  Data collection would be significant in amount with varying types of information required.  In addition, we anticipated that multiple database updates would be implemented in order to refine data collection and the system has demonstrated an ability to accommodate these needs.  While the reporting and metric capabilities do provide some opportunities for future improvements within the software, we can still get to the information.  Overall, our experience has been very positive and we would consider this platform for future studies without hesitation.

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