Unify Trials

Q: What language does Unify Trials support?

Unify Trials supports English,Afrikaans,Arabic,Bengali,Bulgarian,Catalan,Croatian,Czech,Danish,Dutch,Estonian,Filipino,Finnish,French,Ganda,Georgian,German,Greek,Gujarati,Hausa,Hebrew,Hindi,Hungarian,Icelandic,Igbo,Indonesian,Italian,Japanese,Kannada,Kazakh,Kikuyu,Korean,Latvian,Lithuanian,Luxembourgish,Malay,Malayalam,Maltese,Marathi,Norwegian Bokmål,Norwegian Nynorsk,Oriya,Oromo,Polish,Portuguese,Punjabi,Romanian,Russian,Serbian,Sesotho,Simplified Chinese,Slovak,Slovenian,Somali,Spanish,Swahili,Swedish,Tamil,Telugu,Thai,Traditional Chinese,Turkish,Ukrainian,Urdu,Vietnamese,Xhosa,Yoruba,Zulu

Free

9.0.30for iPhone, iPad and more

AstraZeneca Pharmaceuticals LP

Developer

228 MB

Size

Mar 21, 2024

Update Date

Medical

Category

17+

Age Rating

App Store Developer Website

Age Rating

Apps in this category do not contain restricted content.

Apps in this category may contain mild or occasional cartoon, fantasy or real-life violence, as well as occasional or mild adult, sexually suggestive or horrifying content and may not be suitable for children under 9 years of age.

12+

Apps in this category may contain occasional mild indecent language, frequent or intense cartoon or real-life violence, minor or occasional adult or sexually suggestive material, and simulated gambling, and may be for children under 12 years of age.

17+

You must be at least 17 years old to access this App.

Apps in this category may contain frequent and intense offensive language; Frequent and intense cartoon, fantasy or realistic violence: frequent and intense adult, scary and sexually suggestive subjects: as well as sexual content, nudity, tobacco, alcohol and drugs, may not be suitable for children under 17 years of age.

Unify Trials Screenshots

iPad

iPhone

About Unify Trials

The Unify Trials app provides participants in a Clinical trial support and information throughout the trial. Support include reminders for tasks relevant to complete the trial as well as layman information about the relevant disease area and the trial in general. Participants can also provide data through different health questionnaires and other means of data collection. Data can be collected by connected devices in markets and regions where use of devices have regulatory clearance. Use of devices is approved in the US and the EU.