Pharmaceutical Research

Results: 21355



#Item
281Microsoft Word - Savient Receives Complete Response from FDAdoc

Microsoft Word - Savient Receives Complete Response from FDAdoc

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Source URL: www.mvpharm.com

Language: English - Date: 2016-07-11 16:59:30
282Clinical research / Pharmaceutical industry / Clinical trials / Design of experiments / Medical ethics / Informed consent / Case report form / Protocol / Treaty / Clinical research coordinator

ANNEX 1 AF/01-007b/04 Contents of a Submitted Package Protocol Number:……………….. Initial Review Submitted Package Protocol Summary Sheet or Memorandum Application Form for Initial

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Source URL: www.health.gov.bt

Language: English - Date: 2016-06-29 07:05:29
283Practical 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
284Clinical 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
285European 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
286Research  Australian clinical trial activity and burden of disease: an analysis of registered trials in National Health Priority Areas Australian

Research Australian clinical trial activity and burden of disease: an analysis of registered trials in National Health Priority Areas Australian

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Source URL: www.anzctr.org.au

Language: English - Date: 2015-09-13 19:49:14
287Clinical research / Pharmaceutical industry / Clinical data management / Drug safety / Electronic common technical document / Supplementary protection certificate / European Medicines Agency / Summary of Product Characteristics / Pharmacovigilance / Validation / Drug Master File

DOC Document

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Source URL: www.ema.europa.eu

Language: English - Date: 2016-07-20 07:22:57
288POSITION DESCRIPTION Job Title: Clinical Project Management Director  Reports to:

POSITION DESCRIPTION Job Title: Clinical Project Management Director Reports to:

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Source URL: aegleabio.com

Language: English - Date: 2016-06-27 16:08:14
289ACRP_CR_Dec2015_HS_Section.pdf

ACRP_CR_Dec2015_HS_Section.pdf

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Source URL: www.acrpnet.org

Language: English - Date: 2015-11-23 12:15:03
290§ CFR Ch. I (4–1–12 Edition) (3) Requesting that the applicant conduct additional independent studies

§ CFR Ch. I (4–1–12 Edition) (3) Requesting that the applicant conduct additional independent studies

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Source URL: publicfiles.jaeb.org

Language: English - Date: 2014-01-30 11:37:27