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2010
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January
(60)
- Smart Monitor -
- MONITORING_PLAN-locked -
- SDV -
- Regulatory Binder Index Page Device Study.doc -
- Regulatory Binder Table of Contents 3-6-2007 -
- Regulatory Binder Index Drug updated -
- MON FORM 003 Pre Study Qualification Visit Rep...
- cdisc_glossaryterms_version7.1_final_2008 -
- Clinical Research Codes -
- ChecklistRegulatoryBinderReview -
- eCRF -
- demographic form -
- Biochemistry -
- Exclusion -
- inclusion criteria form -
- medical history -
- physical exam -
- randomisation date of visit -
- randomisation -
- What do I Have to Report to the IRB -
- EDC
- Part 2
- ICH-GCP part 1
- Sample Size
- Elements in Informed consent
- Dinesh_20Kumar_20Badyal_Vulnerable_20Clici...
- ICH-CRC-Guide -
- Form 1572
- IND application
- regulations apply to the IND application process
- eCRF Training
- Schedule-Y Indian GCP
- ICH-GCP guidelines
- FAQ s in clinical Research
- protocool -
- sample CRF
- Phases
- sample protocol
- Sulfonylureas Linked to Higher Risks of Death and ...
- Tea, Coffee Seem to Protect Against Diabetes
- Intravitreal Steroids Show Benefit in Diabetic Ret...
- FDA Pleads for More Research on Anemia Drugs
- Informed consent documentation
- Free Clinical Research Book Downloads Free Clinica...
- A Biowaiver means that in vivo bioavailability and...
- Ethics Committee Approval
- Drug Discovery and Drug Development
- Pre clinical Trails
- Clinical trail Phases
- The Role of the CRC in a Clinical Trial
- Group Leader, Clinical Trial Management JOB VAcanc...
- CLINICAL RESEARCH ASSOCIATE (CRA):
- Financial Disclosure by investigators
- Definitions
- Adverse Event Reporting
- Documents required for EC submission
- Institutional Review Board
- Informed Consent for Subject participation in a cl...
- clinical investigator
- clinical Trail protocol
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January
(60)
About Me
- ram
- Hyderabad, Andhra, India
- working as a clinical Research coordinator at yashoda Hospital,Somajiguda,Hyderabad
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