Clinical Data Management

Results: 1569



#Item
101CL UD COMPUTING IN DENTISTRY STARTS  WITH QSIDENTAL

CL UD COMPUTING IN DENTISTRY STARTS WITH QSIDENTAL

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Source URL: www.qsidentalweb.com

Language: English - Date: 2014-08-11 01:21:28
102Deliverable 3.1: State-of-the-art report on standards  Grant Agreement Number: Deliverable number: Deliverable name: Contractual submission date:

Deliverable 3.1: State-of-the-art report on standards Grant Agreement Number: Deliverable number: Deliverable name: Contractual submission date:

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Source URL: p-medicine.eu

Language: English - Date: 2013-02-13 06:22:25
103BOOKS ABOUT QUALITY TRANSMISSION 5R55N  Cityhalllosangeles.com QUALITY TRANSMISSION 5R...

BOOKS ABOUT QUALITY TRANSMISSION 5R55N Cityhalllosangeles.com QUALITY TRANSMISSION 5R...

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Source URL: q.cityhalllosangeles.com

Language: English - Date: 2015-03-05 01:53:21
104Implementation plan for the introduction of the safety features on the packaging of nationally authorised medicinal products for human use Doc. Ref: CMDhFebruary 2016

Implementation plan for the introduction of the safety features on the packaging of nationally authorised medicinal products for human use Doc. Ref: CMDhFebruary 2016

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Source URL: www.hma.eu

Language: English - Date: 2016-02-19 11:51:17
105EU Module 1 Specification - Annex VersionNovember 2011  Document Control

EU Module 1 Specification - Annex VersionNovember 2011 Document Control

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:15:45
106CMD(h) meeting with interested parties

CMD(h) meeting with interested parties

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Source URL: www.hma.eu

Language: English - Date: 2015-05-29 10:17:02
107PRIVACY ANALYTICS DATA SHEET DATA ANONYMIZATION FOR CLINICAL TRIALS

PRIVACY ANALYTICS DATA SHEET DATA ANONYMIZATION FOR CLINICAL TRIALS

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Source URL: www.privacy-analytics.com

Language: English - Date: 2016-03-11 11:10:33
108Practical Guidance For the Paper Submission of Regulatory Information in Support of a Marketing Authorisation Application When Using an eCTD or a NeeS as the Source Submission. v2.0

Practical Guidance For the Paper Submission of Regulatory Information in Support of a Marketing Authorisation Application When Using an eCTD or a NeeS as the Source Submission. v2.0

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:14:51
109Clinical research / Pharmaceutical industry / Clinical data management / Medical ethics / Case report form / Clinical trial / Informed consent / Protocol / Email / Consent

ANNEX 2 AF/02-007b/04 Document Receipt Form Protocol Number: Submitted date: Protocol Version Number:

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Source URL: www.health.gov.bt

Language: English - Date: 2016-06-29 07:05:05
110European Medicines Agency  Evaluation of Medicines for Human Use  London, August 2009  EMEA  V1.0 

European Medicines Agency  Evaluation of Medicines for Human Use  London, August 2009  EMEA  V1.0 

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Source URL: esubmission.ema.europa.eu

Language: English - Date: 2016-08-19 03:14:52