Search Courses and Programs
Use this form to search course ID, name, description, outline, and objectives. This is a multiple word search. Each word must be 3 characters or more (e.g., GMP, GCP, Clinical, etc). Shorter words and any special characters will be ignored. You can search courses for things such as GMP001S1, GAMP, Pharmacovigilance, Quality Assurance, ALCOA, Validation, Clinical Trials, CFR Part 820, Cleaning Validation, or Drug Safety.
Training Programs by Category:
Clinical Research:
For Monitors, Coordinators, Investigators, CROs, & Sponsors
For Monitors, Coordinators, Investigators, CROs, & Sponsors
- Full List: Clinical Research Courses and Programs
- Clinical Trials Management Professional Certification
- Clinical Research Associate (CRA) Professional Certification Program
- Clinical Research Coordinator (CRC) Professional Certification Program
- Good Clinical Practice for Professionals
- GCP & GxP Training Courses for Annual Employee Training
- Safety Reporting in Clinical Trials (Adverse Event Reporting)
- Critical Thinking, Root Cause Analysis, and CAPAs
- Clinical Trials for Regulatory Professionals (Sponsors & CROs)
- Training for Clinical Research Associates (CRAs)
- Training for Clinical Research Coordinators (CRCs)
- Informed Consent: FDA 21 CFR Part 50 Subpart B
- HIPAA & GDPR Training for the Clinical Research Professional
- ISO 14155:2020 – Clinical Research of Medical Devices Standard
Professional Certifications:
Subcategories (Areas of specialty or focus):
cGMP:
Current Good Manufacturing Practice
Current Good Manufacturing Practice
- Full List: cGMP Courses and Programs
- cGMP Professional Certification (Pharmaceuticals)
- cGMP Professional Certification (Medical Devices)
- US Pharmaceutical Quality Assurance (QA) Management Professional Certification Program
- US Medical Device Quality Assurance (QA) Management Professional Certification Program
- FDA Inspection Readiness for Professionals
- cGMP for Intermediate Professionals
- cGMP and GxP Refresher Courses for Annual Employee Training
- cGMP and GxP for Beginners (Onboarding new Employees)
- cGMP: Quality Assurance and Quality Control
- cGMP for Intermediate Employees
- cGMP for Advanced Employees (Pharmaceuticals)
- cGMP for Advanced Employees (Medical Devices)
- cGMP for Combination Products – Pharmaceuticals & Medical Devices
- Change Control
- Root Cause Analysis & CAPA
- FDA Inspection Readiness (GMP Auditing)
- FDA 21 CFR Part 211 Courses (Pharmaceuticals)
- FDA 21 CFR Part 820 Courses (Medical Devices)
- CFDA: China Food and Drug Administration (GMP for Medical Devices)
Professional Certifications:
Subcategories (Areas of specialty or focus):
GLP:
Good Laboratory Practice & ALCOA
Good Laboratory Practice & ALCOA
- Full List: Good Laboratory Practice (GLP) Courses and Programs
- GLP: Good Laboratory Practice Professional Certification Program
- GLP: Data Integrity & ALCOA
- GLP: Preparing for Audits
- GLP: Organization, Roles, & Infrastructure
- Contamination Control & Aseptic Techniques
- Pharmaceutical Microbiology
Professional Certification:
Subcategories (Areas of specialty or focus):
Microbiology:
Contamination Control & Aseptic Techniques
Contamination Control & Aseptic Techniques
- Full List: Microbiology & Contamination Control Courses and Programs
- Pharmaceutical Microbiology Professional Certification Program
- Pharmaceutical Contamination Control Professional Certification Program
- Pharmaceutical Microbiology
- Contamination Control and Aseptic Techniques
- GLP: Good Laboratory Practice
Professional Certifictions:
Subcategories (Areas of specialty or focus):
Drug Safety:
Pharmacovigilance, Pharmacokinetics, & Pharmacodynamics
Pharmacovigilance, Pharmacokinetics, & Pharmacodynamics
- Full List: Drug Safety, Pharmacovigilance, Pharmacokinetics, and Pharmacodynamics Courses and Programs
- Drug Safety and Pharmacovigilance Professional Certification Program
- Good Pharmacoepidemiology Practice Professional Certification Program
- Pharmacokinetics and Pharmacodynamics for Professionals
- Introduction to Drug Safety and Pharmacovigilance
- Safety Reporting in Clinical Trials (Adverse Event Reporting)
- GPP: Good Pharmacoepidemiology Practice
- Conducting Pharmacokinetic and Pharmacodynamic Studies
- Pharmacokinetics and Pharmacodynamics in Drug Development & Registration
Professional Certifications:
Subcategories (Areas of specialty or focus):
Data Integrity & GDocP:
Good Documentation Practice & ALCOA
Good Documentation Practice & ALCOA
- Full List: Data Integrity & Good Documentation Practice (GDocP) Courses
- Data Integrity Professional Certification Program
- Good Documentation Practices (GDocP) Professional Certification Program
- Data Integrity (ALCOA and ALCOA+)
- GDocP: Good Documentation Practice
- SOPs: How to Write Effective Standard Operating Procedures
- URS: How to Write an Effective Equipment User Requirement Specification
- FDA 21 CFR Part 11: Electronic Records & Electronic Signatures
Professional Certifications:
Subcategories (Areas of specialty or focus):
FDA 21 CFR Part 11:
Electronic Records & Electronic Signatures
Electronic Records & Electronic Signatures
- Full List: 21 CFR Part 11 Courses and Programs
- 21 CFR Part 11 Professional Certification
- Compliance with Regulation 21 CFR Part 11 (Electronic Records and Electronic Signatures)
- 21 CFR Part 11: An Introduction
- 21 CFR Part 11: Electronic Signatures
Professional Certification:
Subcategories (Areas of specialty or focus):
Medical Devices:
GMP, Audits, Validation, & Regulatory Affairs
GMP, Audits, Validation, & Regulatory Affairs
- Full List: Medical Devices Courses and Programs
- US Medical Device Quality Assurance (QA) Management Professional Certification Program
- FDA 21 CFR Part 820: Medical Device cGMP Professional Certification Program
- ISO 13485:2016 Professional Certification Program
- EU Medical Device Regulation (EU MDR) for Professionals
- Medical Device Single Audit Program (MDSAP) for Professionals
- Medical Device Validation for Professionals
- Regulatory Affairs: Introduction to the Regulation of Medical Devices
- EU MDR: EU Medical Device Regulation
- MDSAP: Medical Device Single Audit Program
- FDA 21 CFR Part 820: US cGMP for Medical Devices
- FDA Inspection Readiness (GMP Auditing)
- ISO 14971:2019 Medical Devices
- ISO 13485:2016 Medical Devices
- ISO 14155:2020 Clinical Research of Medical Devices Standard
- Validation: Medical Devices
- Change Control
- Root Cause Analysis & CAPA
- cGMP and GxP Refresher Courses for Annual Employee Training
- cGMP and GxP for Beginners (Onboarding new Employees)
- cGMP for Intermediate Employees
- cGMP for Advanced Employees
- cGMP for Combination Products: Pharmaceuticals & Medical Devices
- China CFDA: cGMPs
Professional Certifications:
Subcategories (Areas of specialty or focus):
OSHA and HR EEO:
Safety Training for Healthcare, Clinical, & Medical Professionals
Safety Training for Healthcare, Clinical, & Medical Professionals
- Full List: OSHA for Healthcare / Medical Professionals
- OSHA for Healthcare Professionals
Full List: HR/EEO for Employees and Managers
Professional Program:
Quality Assurance (QA):
Pharmaceuticals & Medical Devices
Pharmaceuticals & Medical Devices
- Full List: Quality Assurance (QA) Courses and Programs
- US Pharmaceutical Quality Assurance (QA) Management Professional Certification Program
- US Medical Device Quality Assurance (QA) Management Professional Certification Program
- cGMP Professional Certification (Pharmaceuticals)
- cGMP Professional Certification (Medical Devices)
- cGMP: Quality Assurance and Quality Control (QA/QC)
- Root Cause Analysis & CAPA
- FDA 21 CFR Part 211: US cGMP for Pharmaceuticals
- FDA 21 CFR Part 820: US cGMP for Medical Devices
- ISO 13485:2016 Chapter 4: The Quality Management System (QMS)
- ISO 13485:2016 Measurement Analysis and Improvement (Chapter 8, Part B)
Professional Certifications:
Subcategories (Areas of specialty or focus):
Regulatory Affairs:
Pharmaceuticals, Medical Devices, & Clinical Research
Pharmaceuticals, Medical Devices, & Clinical Research
- Full List: Regulatory Affairs Courses and Programs
- Global Pharmaceutical Regulatory Affairs Professional Certification Program
- US Pharmaceutical Regulatory Affairs Professional Certification Program
- Clinical Trials Management (US & EU) Professional Certification Program
- Obtaining Approval for Clinical Trials in US & EU for Professionals
- EU MDR: EU Medical Device Regulation for Professionals
- Medical Device Single Audit Program (MDSAP) for Professionals
- Introduction to the Regulation of Medical Devices
- Regulatory Affairs for Human Medicinal Products (EU and US)
- MRP – The Mutual Recognition Procedure
- CTD – Preparing Submissions in the Common Technical Document Format
- eCTD – Electronic Common Technical Document
- DCP – The Decentralized Procedure
- NDA – Submitting a New Drug Application: Obtain Approval to Market in the US
- Registration of Drugs Based on Monoclonal Antibodies
- How to Gain Approval to Market Generic Drugs in the US
- The Regulatory Pathway to Licensing Follow-on Biologics (Biosimilars) in the USA
Professional Certifications:
Subcategories (Areas of specialty or focus):
Selling and Marketing:
Pharmaceuticals in the USA
Pharmaceuticals in the USA
- Full List: Pharmaceutical Sales and Marketing
- Pharmaceutical Sales & Marketing Professional Certification
- Legal and Regulatory Framework for Advertising and Promotion of Prescription Drugs in the USA
- Regulatory Requirements and Guidance on Advertising and Promotion of Prescription Drugs in the USA
- Consumer-directed Advertising and Online Promotion of Prescription Drugs in the USA
- Marketing of Prescription Drugs in the USA- Interactions with Healthcare Professionals
Professional Certification:
Subcategories (Areas of specialty or focus):
Validation:
Computer, Software, Process, Equipment, & Qualification
Computer, Software, Process, Equipment, & Qualification
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Full List: Validation Courses and Programs
- Pharmaceutical Validation Management Professional Certification Program
- CSV: Computer System Validation Professional Certification
- SVA: Software Validation Assurance Professional Certification
- Process Validation for Professionals
- Medical Device Validation for Professionals
- Equipment Qualification for Professionals
- Process Validation
- Change Control
- Root Cause Analysis & CAPA
- Validation for Medical Devices
- Equipment Qualification
- SVA: Software Validation Assurance
- CSV: Computer System Validation for Beginners
- CSV: Computer System Validation for Intermediates
Full List: CSV: Computer System Validation Courses and Programs
Professional Certifications:
Subcategories (Areas of specialty or focus):
