'Ich gcp' diaporamas de présentation

Good Clinical Practice (GCP) A whistle stop tour!

1.32k views • 86 slides

Research Guidelines

Research Guidelines. Research Governance EU Directive on Clinical Trials ICH-GCP: Informed Consent Safety & Adverse Events Documentation - Audit. ICH definition - GCP.

815 views • 70 slides

Planning a BE Study

875 views • 62 slides

Clinical Trial Regulations

Clinical Trial Regulations. P.Olliaro Nov04. Clinical Trials: a Phase of Product Development. R&D ATTRITION RATES. < discovery >. <pre-clinical>. < clinical >. MARKETING. DISCOVERY. REGULATORY REVIEW. PRE-DEVELOPMENT. IND filing. NDA filing. DEVELOPMENT.

1.27k views • 61 slides

Clinical Trial Regulations

Clinical Trial Regulations. P.Olliaro Nov04. Clinical Trials: a Phase of Product Development. R&D ATTRITION RATES. < discovery >. <pre-clinical>. < clinical >. MARKETING. DISCOVERY. REGULATORY REVIEW. PRE-DEVELOPMENT. IND filing. NDA filing. DEVELOPMENT.

956 views • 61 slides

GCP for Emergency Medicine

GCP for Emergency Medicine. GCP for Emergency Medicine. This presentation is intended for emergency physicians involved in recruiting patients to clinical trials and/or caring for patients who are in clinical trials

839 views • 56 slides

708 views • 56 slides

GCP for Emergency Medicine

GCP for Emergency Medicine. GCP for Emergency Medicine. This presentation is intended for emergency physicians involved in recruiting patients to clinical trials and/or caring for patients who are in clinical trials

572 views • 56 slides

Complexity of the insulin signaling pathway

IRS1. IRS2. IRS3. p85 ?. p110 ?. p55 ?. IRS4. p110 ?. p50 ?. p110 ?. p85 ?. p55 ?. Complexity of the insulin signaling pathway. Insulin. TNF ?. Cytokines. IGF1. Plasma membrane. TNFR. Rec. IGF1R. PTP1B. CAP. Shc. Jak. cbl. Jnk. Rac. cdc42. Stat. ?. ?. PTEN. PDK 1,2.

615 views • 39 slides

Quality and Documentation Tips for Compliance

Quality and Documentation Tips for Compliance. Janet Ellen Holwell, CCRC, CCRA President, NY Metropolitan Chapter of ACRP. Key learning objectives. By the end of this module you should be able to: Recognize the importance of quality in clinical trials

489 views • 35 slides

Research involving cognitively impaired persons

Research involving cognitively impaired persons. Chin Jing Jih Adjunct Assoicate Professor, NUS Centre for Biomedical Ethics Programme Director, NHG Research Quality Assurance Deputy Co-Chair, NHG Research Ethics Committee. Outline. Definition of cognitive impairment

497 views • 32 slides

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DIA Trial Master File Reference Model

DIA Trial Master File Reference Model. EDM Reference Model. DIA Document and Records Management Special Interest Area Community initiative since 2008 Standardization effort for the industry with eCTD backbone Version 1 launched in 2008, update in the works

1.04k views • 15 slides

Understanding GCP: education, training and experience

341 views • 14 slides

Best clinical research partner preparing in Pune

Clinical research partner is continually being a screen who is being checking the preliminary all through the investigation.

51 views • 3 slides

Best clinical research accomplice planning in Pune

Clinical research accomplice is persistently being a screen who is being checking the starter all through the examination.

42 views • 3 slides