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ERT eCOA Handheld4.7

The ERT eCOA BYOD App is intended for use by patients, caregivers, or site personnel to collect data relating to a clinical trial

Ellodi eCOA App is intended for use of collecting patient reported outcomes relating to the SP-1011-005 Study

Zosano Cluster Study-

Zosano Pharma Cluster Study eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

VALIANT diary (APL2-C3G-310)-

The VALIANT and VALE study diaries are for participants in a clinical trial to record study related activities and outcomes.

U & Resolution-

Lundbeck Resolution eCOA App is intended for use to collect patient-reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Upstream Bio VIBRANT-

The Upstream Bio VIBRANT eCOA App is intended for use to collect patient reported outcomes relating to the UPB-CP-03 clinical trial. Patients must be given accounts by a participating site in order to log in to the app

Lundbeck U&DELIVER eCOA App is intended for use to collect patient-reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Takeda_TAK-788-3001-

Takeda eCOA App is intended for use to collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Takeda TAK-101-2001-

Takeda eCOA App is intended for use to collect patient reported outcomes relating to the TAK-101-2001 clinical trial. Patients must be given accounts by a participating site staff member in order to log in to the app.

ReViral REVC006-

ReViral REVC006 eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Sanofi VAT00008-

Sanofi VAT00008 eCOA App is intended for use to collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Reata CYPRESS 901-C-2102-

Reata eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Restricted-use questionnaire for patients living with PD.

OM Pharma BV-2020/09 - EAGLE-

OM Pharma eCOA App is intended for collecting patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

NOVONOR_NN7415-4307-

The Novo Nordisk eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

MS202359_0002 (Xray Vision)-

The MS202359_0002 eCOA App is intended for use collecting patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

MSD MK5684-01A eCOA App is intended for use collect patient reported outcomes relating to MK5684-01A clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

MSD MK5684-004 eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app

MSD MK5684-003 eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Mirum MRX 800 MERGE-

Mirum eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Meiji Pharma/Syneos_ME3183-5-

Meiji Pharma/Syneos Health_ME3183-5 eCOA App is intended for use and collection of patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Marinus TrustTSC-

The Marinus TrustTSC study diary is for participants to record seizure activity and medication use daily during study participation. This app allows you to answer daily diary questions, enter seizures, enter medication use, and set up alert/reminder/notification preferences.

Landos NX-13-201 Nexus-

The Landos eCOA App is intended for use collect patient reported outcomes relating to the NX-13-201 clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Janssen VAC18195RSV1001-

The Janssen eCOA App is intended for use collect patient reported outcomes relating to the VAC18195RSV1001 clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Janssen_REASON CNTO1959CRD3008-

Janssen eCOA App is intended for use to collect patient reported outcomes relating to the CNTO1959CRD3008 – REASON clinical trial. Patients must be given accounts by a participating site staff member in order to log in to the app.

Janssen E.ngage-

The Janssen eCOA App is intended for use collect patient reported outcomes relating to the VAC52416BAC3002 / E.ngage clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Janssen E.mbrace-

Janssen eCOA App is intended for use to collect participant reported outcomes relating to a clinical trial. Participants must be given accounts by a participating site in order to log in to the app.

Janssen 61186372NSC2007 COCOON-

The Janssen eCOA App is intended for use to collect patient reported outcomes relating to the 61186372NSC2007 (COCOON) clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Janssen 40411813EPY2001-

The Janssen COA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

InflaRx eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

IMVT-1401-2401-

The Immunovant eCOA App is intended for use to collect weekly study dosing information in a dosing diary relating to the IMVT-1401-2401 clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Immorna – JCXH-

Study diary is for participants to record side effects that occur after study vaccine administration (JCXH-105 or Shingrix). This app allows you to answer diary questions, enter side effects and set up alert/reminder/notification preferences.

Icosavax ICVX-12-201-

Icosavax eDiary App is intended for use to collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

ICON P1-CVD-05-

ICON P1-CVD-05 eCOA App is intended for use to collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app

ICON P1-COPD-04-INT-

ICON P1-COPD-04-INT eCOA App is intended for use to collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

HERMES Study App EX6018-4915-

The HERMES Study App EX6018-4915 will collect dosing information as well as patient reported outcomes for a clinical trial. Sites participating in the clinical trial are required to create accounts for each patient in the HERMES Study App EX6018-4915 before patients can log into the App.

GSK TH HSV REC 003-

GSK eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app

GSK MENABCWY-020 eDiary-

GSK eCOA App is intended for use in collecting patient-reported outcomes relating to a clinical trial.

GSK EPI HSV 006 BOD TH-

GSK eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

GSK 217043 eDiary-

GSK eCOA App is intended for use in collecting patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Escient EP-262-202-

Escient Pharmaceuticals eCOA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

ePRO BI1403-0008-

Boehringer Ingelheim ePRO BI1403-0008 is intended to collect patient reported outcomes relating to a clinical trial (BI Trial 1403-0008 – Brightline-1). Patients must be given accounts by a participating site in order to log in to the app.

EP-547-201 (PACIFIC)-

Escient Pharmaceuticals eCOA App is intended for use to collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Enanta_EDP938104-

The Enanta eCOA App is intended for use collect patient reported outcomes relating to the EDP938104 clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

This eCOA App is intended for use collect patient reported outcomes (ePRO) relating to the Emerald-3 clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

Eli Lilly J2A-MC-GZGV-

Eli Lilly J2A-MC-GZGV eCOA App is intended for use to collect patient-reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

EDiary Abliva Falcon Study-

Abliva eCOA App is intended for use to collect patient reported outcomes relating to Abliva's clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

An app for the TAK-660-403 Protocol. Evaluation of long-term safety of ADYNOVI / ADYNOVATE(Antihaemophilic Factor [Recombinant] PEGylated, rurioctocog alfa pegol) in patients with haemophilia A – An ADYNOVI / ADYNOVATE Post-Authorisation Safety Study (PASS)

ENABLE (SHP643-402)-

A three-year, non-interventional, prospective, multicenter study to evaluate the long-term effectiveness of lanadelumab in real-world clinical practice (ENABLE)

Sanofi VAD00001 Digital Patient App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

This study application has been developed for use on the PSK00008 vaccine study.

This study application has been developed for use on the HSV15 vaccine study being conducted in the United States, to assess the safety, immunogenicity and efficacy of the vaccine in healthy adult subjects.

The Hydration Diary is for patients participating in the Dragonfly Therapeutics, Inc. DF6215-001 study. The purpose of the Hydration Diary is to collect patient's daily fluid intake to support protocol compliance. Patients should seek a doctor's advice in addition to this app before making any medic

Dare eDIARY App is intended for use to collect patient-reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

CSL Seqirus V205_01-

CSL Seqirus eCOA App is intended for use of collecting patient reported outcomes relating to the V205_01 Study

CSL Seqirus V204_01-

CSL Seqirus eCOA App is intended for use of collecting patient reported outcomes relating to the V204_01 Study

CSL_IgPro20_3010-

The CSL Behring CSL_IgPro20_3010 App is intended for use to collect patient reported outcomes relating to the CSL_IgPro20_3010 clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

CSL Behring CSL222_3005-

The CSL Behring COA App is intended for use collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to login to the app.

CSL Behring CSL222_3002-

The CSL Behring COA App is intended for use of collecting patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to login to the app.

CSL312_3003 eCOA App is intended for use to collect patient reported outcomes relating to a clinical trial. Patients must be given accounts by a participating site in order to log in to the app.

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