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Special Topics in Clinical Research
Evidence Based Medicine
Mastering Critical Appraisal of Study Designs
How to Critically Appraise Scientific Articles
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The Art of Addressing Reviewer’s Comments in Scientific Journals
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Patient Experience Foundations for Healthcare Professionals
Quality and Accreditation in Healthcare
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Lean in Healthcare
Root Cause Analysis and FMEA
Writing Effective Policies and Procedures in Healthcare
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Hospital Accreditation: Effective Implementation and Efficient Sustainability
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Biostatistics for Non-Statisticians
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Introduction to Research and Medical Ethics
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New Drug Development Process
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Clinical Trial Protocol Development and Write-Up
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Clinical Trial Agreements (CTAs)
Medical Writing of Clinical Trial Documents
Epidemiology
Epidemiology: The Basic Science of Public Health
The Clinical Research Process from Initiation to Publication
Study Designs: Methodology and Interpretation
Introduction to Systematic Reviews and Meta-Analyses
Good Practice Training “GXP”
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GMP – Good Manufacturing Practice
GLP – Good Laboratory Practice
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GDP – Good Distribution Practice
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Essentials of Grant Proposal Development and Write-Up
Write-Up of a National Formulary
Medical Writing of Clinical Trial Documents
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Charge Nurse Master Class
Patient Experience Foundations for Healthcare Professionals
Telehealth Excellence: The Future of Work in Healthcare
Generalities
The EU New Clinical Trial Regulation (EU) No 536/2014 – Basics and Implementation
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Healthcare Professionals
CPHQ Preparatory Course
Telehealth Excellence: The Future of Work in Healthcare
Lean in Healthcare
Good Clinical Practice - GCP
Root Cause Analysis and FMEA
Clinical Research Associate (CRA) - Foundations
Patient Experience Foundations for Healthcare Professionals
Academic and Regulatory Medical Writing
Hospital Accreditation
Wound Care Management Program
Hospital Accreditation: Effective Implementation and Efficient Sustainability
Distruptive Innovation in Healthcare
Healthcare Information System
Healthcare Digital Business & Marketing
Epidemiology: The Basic Science of Public Health
The Clinical Research Process from Initiation to Publication
Study Designs: Methodology and Interpretation
Introduction to Systematic Reviews and Meta-Analyses
Essentials in Biostatistics
Introduction to Research and Medical Ethics
Institutional Review Board (IRB) Administration
Responsible Conduct of Research (RCR)
Good Clinical Practices (GCP) for Clinical Trials with Investigational Drugs
Essentials of Grant Proposal Development and Write-Up
Write-Up of a National Formulary
Medical Writing of Clinical Trial Documents
New Drug Development Process
Clinical Trial Planning: Design, Protocol Development, Data Management and Clinical Site Activities
Clinical Trial Protocol Development and Write-up
Medical Writing of Clinical Trial Documents
Clinical Trial Agreements (CTAs)
GMP – Good Manufacturing Practice
GLP – Good Laboratory Practice
GVP – Good Pharmacovigilance Practice
GPP - Good Pharmacy Practice
GDocP - Good Documentation Practice
GDP – Good Distribution Practice
Writing Effective Policies and Procedures in Healthcare
The EU New Clinical Trial Regulation (EU) No 536/2014 – Basics and Implementation
Evidence Based Medicine
Mastering Critical Appraisal of Study Designs
How to Critically Appraise Scientific Articles
The Publication Process in Scientific Journals
The Art of Addressing Reviewer’s Comments in Scientific Journals
Pharmacovigilance Fundamentals
Medical Doctors
Clinical Research Associate (CRA) - Foundations
CPHQ Preparatory Course
Good Clinical Practice - GCP
Epidemiology: The Basic Science of Public Health
The Clinical Research Process from Initiation to Publication
Essentials in Biostatistics
Introduction to Research and Medical Ethics
Responsible Conduct of Research (RCR)
Institutional Review board (IRB) Administration
Good Clinical Practices (GCP) for Clinical Trials with Investigational Drugs
Essentials of Grant Proposal Development and write-up
Write-Up of a National Formulary
Medical Writing of Clinical Trial Documents
New Drug Development Process
Clinical Trial Planning: Design, Protocol Development, Data Management and Clinical Site Activities
Clinical Trial Protocol Development and Write-Up
Essentials of Grant Proposal Development and Write-Up
Medical Writing of Clinical Trial Documents
Clinical Trial Agreements (CTAs)
Good Clinical Practice - GCP
GVP – Good Pharmacovigilance Practice
GDocP - Good Documentation Practice
Evidence Based Medicine
Mastering Critical Appraisal of Study Designs
How to Critically Appraise Scientific Articles
The Publication Process in Scientific Journals
The Art of Addressing Reviewer’s Comments in Scientific Journals
Pharmacovigilance Fundamentals
Conference Presentation Skills and Preparation steps for Researchers
Patient Experience Foundations for Healthcare Professionals
Pharmacists
GVP – Good Pharmacovigilance Practice
GPP - Good Pharmacy Practice
GDocP - Good Documentation Practice
GDP – Good Distribution Practice
The EU New Clinical Trial Regulation (EU) No 536/2014 – Basics and Implementation
Evidence Based Medicine
Mastering Critical Appraisal of Study Designs
How to Critically Appraise Scientific Articles
The Publication Process in Scientific Journalse
The Art of Addressing Reviewer’s Comments in Scientific Journals
Conference Presentation Skills and Preparation Steps for Researchers
Pharmacovigilance Fundamentals
Medical Representative Academy
Nurses
Wound Care Program
Nursing Executive Program
Charge Nurse Master Class
CPHQ Preparatory Course
Telehealth Excellence: The Future of Work in Healthcare
Lean in Healthcare
Root Cause Analysis and FMEA
Writing Effective Policies and Procedures in Healthcare
Hospital Accreditation
Hospital Accreditation: Effective Implementation and Efficient Sustainability
Medical Laboratory Technicians
CPHQ Preparatory Course
Lean in Healthcare
Root Cause Analysis and FMEA
Writing Effective Policies and Procedures in Healthcare
GLP – Good Laboratory Practice
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Nursing Executive Program
Capacity Building program for Hospitals and Medical Centers
Mastering Clinical Research: Training Program for Doctors
Building a Quality and Safety Resource Center
Medical Representative Academy
Mastering Clinical Research: Training Program for Pharmaceutical Companies
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Home
About
About Osten Healthcare
Meet our Course Directors
Certificates and Accreditations
Courses By Topics
Biostatistics
Clinical Programs in Healthcare
Clinical Research and Medical Ethics
Clinical Trial Foundation
Epidemiology
Good Practice Training “GXP”
Healthcare Technology and Digitalization
Medical Writing
Nursing Capacity Building
Quality and Accreditation in Healthcare
Special Programs
Special Topics in Clinical Research
Generalities
Courses By Speciality
Healthcare Professionals
Medical Doctors
Nurses
Medical Laboratory Technicians
All Courses
Special Programs
Nursing Executive Program
Capacity Building Program for Hospitals and Medical Centers
Mastering Clinical Research: Training Program For Doctors
Building a Quality and Safety Resource Center
Medical Representative Academy
Mastering Clinical Research: Training Program for Pharmaceutical Companies
Contact
Contact Us
Join Our Team
Epidemiology
Epidemiology: The Basic Science of Public Health
The Clinical Research Process from Initiation to Publication
Study Designs: Methodology and Interpretation
Introduction to Systematic Reviews and Meta-Analyses