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Complete List of Archived Courses and Professional Training Programs

Certification Training

Understanding Anti-Bribery and Anti-Corruption – ABAC01

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Certification Training

Good Laboratory Practice (GLP) Professional Certification Program – GLPPRO

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Certification Training

US Pharmaceutical Quality Assurance (QA) Management Professional Certification Program – QAPRO

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Certification Training

US Medical Device Quality Assurance (QA) Management Professional Certification Program – QADPRO

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Certification Training

21 CFR Part 211: Good Manufacturing Practice Professional Certification Program – GMPP11

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Certification Training

21 CFR Part 820: Medical Device cGMP Professional Certification Program – MDPRO

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Certification Training

Good Distribution Practices (GDP) Professional Certification Program – GDPro

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Certification Training

Good Pharmacovigilance Practices (GVP) Professional Certification Program – GVPro

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Certification Training

Data Integrity Professional Certification Program – DATAINT

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Certification Training

Good Documentation Practices (GDocP) Professional Certification Program – GDOCP

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Certification Training

21 CFR Part 11 – Electronic Records & Signatures Professional Certification Program – ESRPRO

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Certification Training

Pharmaceutical Microbiology Professional Certification Program – PMPCERT

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Certification Training

Pharmaceutical Contamination Control Professional Certification Program – PCCP

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Certification Training

Computer System Validation (CSV) Professional Certification Program – CSVPRO

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Certification Training

Computer Software Assurance (CSA) Professional Certification Program – SVPRO

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Certification Training

ISO 13485:2016 Professional Certification Program – ISOPCRT

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Certification Training

Change Control Professional Certification – CCPRO

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Certification Training

ISO 14971:2019 for Professionals – ISOPRO

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Certification Training

EU Medical Device Regulation (EU MDR) for Professionals – EUMDR

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Certification Training

Medical Device Single Audit Program (MDSAP) for Professionals – MDSAP

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Certification Training

cGMP for Beginning Professionals – GMPBEGP

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Certification Training

cGMP for Intermediate Professionals – GMPINTP

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Certification Training

GMP Auditor Professional Certification Program – AUDPro

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Certification Training

FDA Inspection Readiness for GMP Auditors and Professionals – FDAINSP

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Certification Training

cGMP: Combination Products for Professionals – COMPR

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Certification Training

Good Clinical Practice for Professionals – GCPFP

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Certification Training

Informed Consent of Human Subjects (HSP) for Professionals – INFCON

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Certification Training

Computer Software Validation for Beginning Professionals – CSVBEG

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Certification Training

Medical Device Validation for Professionals – MDVAL

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Certification Training

Equipment Qualification for Professionals – EQPRO

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Certification Training

Process Validation for Professionals – PVPRO

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Certification Training

ICH E6(R2) – Clinical Trial Protocol and Protocol Amendment (Chapter 6) – ELM-915

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Certification Training

ICH E6(R2) – Introduction and Principles of Good Clinical Practices (GCP) (Chapter 1-2) – ELM-904

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Certification Training

ICH E6(R2) – Institutional Review Board / Independent Ethics Committee (IRB/IEC) (Chapter 3) – ELM-924

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Certification Training

Clinical Trials: 21 CFR Part 50 Subpart B – Informed Consent of Human Subjects (HSP) [Part 1 of 2] – ELM-909

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Certification Training

Clinical Trials: 21 CFR Part 50 Subpart B – Informed Consent of Human Subjects (HSP) [Part 2 of 2] – ELM-910

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Certification Training

GCP: An Introduction to Good Clinical Practices – Part 1 of 3 – ELM-901

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Certification Training

GCP: An Introduction to Good Clinical Practices – Part 2 of 3 – ELM-902

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Certification Training

GCP: An Introduction to Good Clinical Practices – Part 3 of 3 – ELM-903

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Certification Training

Contamination Prevention and Control in a GMP Environment – ELM-105

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Certification Training

Introduction to Cleaning Validation – ELM-601

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Certification Training

Types of Contamination in a GMP Environment – ELM-701

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Certification Training

Sources of Contamination in a GMP Environment – ELM-702

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Certification Training

Contamination Prevention and Control – Quality Risk Management (QRM) – ELM-703

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Certification Training

Contamination Control Strategies in a GMP Environment – ELM-704

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Certification Training

The Basic Principles of Isolator Technology – ELM-707

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Certification Training

Restricted Access Barrier Systems (RABS) Glove Training – ELM-708

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Certification Training

Introduction to Endotoxin Control – ELM-709

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Certification Training

How Deviations (Non-Conformance) Should be Handled from a Regulatory Perspective – ELM-712

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Certification Training

Pharmaceutical Contamination and Microorganisms – ELM-713

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Certification Training

Sources of Pharmaceutical Contamination – ELM-714

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Certification Training

The Use of Vaporized Hydrogen Peroxide (VHP) Chambers – ELM-715

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Certification Training

Contamination Control Strategies in a GMP Environment: Cleaning and Disinfection – ELM-716

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Certification Training

Pharmaceutical Microbiology and Industry Considerations – ELM-711

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Certification Training

Microbiological Testing Methods – ELM-721

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Certification Training

Microbial Contamination of Pharmaceutical Products – Part 1 – ELM-705

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Certification Training

Microbial Contamination of Pharmaceutical Products – Part 2 – ELM-706

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Certification Training

Control of Microbiological Contamination in a GMP Environment – ELM-720

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Certification Training

Microbiological Environmental Monitoring – ELM-719

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Certification Training

GMP Contamination Control Strategies – Personnel – ELM-717

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Certification Training

GMP Contamination Control Strategies – Buildings and Facilities – ELM-718

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Certification Training

Good Pharmacovigilance Practices (GVP): An Introduction to Pharmacovigilance and Adverse Drug Reaction – ELM-920

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Certification Training

Good Pharmacovigilance Practices (GVP): Legal Framework of the Global Pharmacovigilance Program – ELM-921

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Certification Training

Good Pharmacovigilance Practices (GVP): Updates to the European Union GVP Guidelines – ELM-922

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Certification Training

Good Pharmacovigilance Practices (GVP): Recent Inspections and Warning Letter Case Studies – ELM-923

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Certification Training

GLP: An Introduction to Good Laboratory Practices (GLP) – ELM-101

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Certification Training

GLP: Laboratory Data Integrity and the Principles of ALCOA (GDocP) – ELM-102

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Certification Training

GLP: How to Prepare for Internal & External Laboratory Audits – ELM-106

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Certification Training

GLP: Laboratory Investigations & Deviations – ELM-108

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Certification Training

GLP: Performing Analytical Analysis in a Regulated Laboratory – ELM-109

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Certification Training

GLP: Organization, Roles and Infrastructure for Regulated or Accredited Laboratories – ELM-110

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Certification Training

GLP: The Basics of Laboratory Investigations – ELM-174

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Certification Training

GLP: How to Conduct a Laboratory Investigation – ELM-175

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Certification Training

GMP: Introduction to Good Manufacturing Practices (For Beginners) – ELM-722

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Certification Training

GMP: The Devastating Effects of Not Following cGMP (For Beginners) – ELM-710

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Certification Training

GMP: Good Manufacturing Practices – ELM-103

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Certification Training

GMP: Cases from History and the Regulations – ELM-201

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Certification Training

GMP: Good Manufacturing Practices – QMS, Premises and Personnel – ELM-202

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Certification Training

GMP: Equipment, Validation, Complaints and Self Inspection – ELM-203

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Certification Training

GMP: Good Manufacturing Practices – Good Practices and Quality Control – ELM-204

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Certification Training

GMP: 21 CFR Part 211 Subpart B – Organization and Personnel – ELM-211

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Certification Training

GMP: 21 CFR Part 211 Subpart C – Building and Facilities – ELM-205

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Certification Training

GMP: 21 CFR Part 211 Subpart D – Equipment – ELM-212

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Certification Training

GMP: 21 CFR Part 211 Subpart E – Control of Components, Drug Product Containers and Closures – ELM-206

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Certification Training

GMP: 21 CFR Part 211 Subpart F – Production and Process Controls – ELM-208

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Certification Training

GMP: 21 CFR Part 211 Subpart G – Packaging and Labeling Control – ELM-209

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Certification Training

GMP: 21 CFR Part 211 Subpart H – Holding and Distribution – ELM-207

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Certification Training

GMP: 21 CFR Part 211 Subpart J – Records and Reports – ELM-210

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Certification Training

GMP: 21 CFR Part 211 Subpart K – Returned and Salvaged Drug Products – ELM-213

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Certification Training

GMP: Behavioral Based Quality (BBQ) for a GMP Environment – ELM-120

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Certification Training

GMP: Combination Products (Drugs, Devices and Biologics) – Part 1 of 3 – ELM-145

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Certification Training

GMP: Combination Products (Drugs, Devices and Biologics) – Part 2 of 3 – ELM-146

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Certification Training

GMP: Combination Products (Drugs, Devices and Biologics) – Part 3 of 3 – ELM-147

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Certification Training

GMP: FDA Inspection Readiness- How to be an Effective GMP Auditor (Part 1 of 3) – ELM-122

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Certification Training

GMP: FDA Inspection Readiness- How to be an Effective GMP Auditor (Part 2 of 3) – ELM-123

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Certification Training

GMP: FDA Inspection Readiness- How to be an Effective GMP Auditor (Part 3 of 3) – ELM-124

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Certification Training

General GMP Inspection Readiness – ELM-190

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Certification Training

GMP Inspection Readiness: Your Role & Preparing for Inspector Interactions – ELM-191

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Certification Training

GMP: China Food and Drug Administration (CFDA) – GMP for Medical Devices – ELM-330

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Certification Training

GMP: China Food and Drug Administration (CFDA) – GMP for Implantable Medical Devices – ELM-331

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Certification Training

ISO 14971:2019 – The Scope of the Standard – ELM-333

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Certification Training

ISO 14971:2019 – The Evolution and Definitions – ELM-334

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Certification Training

ISO 14971: Basic Framework for Risk Management – ELM-335

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Certification Training

ISO 14971: Characterizing the Device & Identifying Hazards – ELM-336

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Certification Training

ISO 14971: Risk Analysis, Evaluation & Control – ELM-337

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Certification Training

ISO 14971: Different Perspectives of a Risk Management Program – ELM-338

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Certification Training

ISO 13485:2016 – Chapter 1-3: Introduction – ELM-801

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Certification Training

ISO 13485:2016 – Chapter 4: The Quality Management System (QMS) – ELM-802

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Certification Training

ISO 13485:2016 – Chapter 5: Management Responsibility – ELM-803

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Certification Training

ISO 13485:2016 – Chapter 6: Resource Management – ELM-804

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Certification Training

ISO 13485:2016 – Product Realization (Chapter 7 – Part A) – ELM-805

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Certification Training

ISO 13485:2016 – Product Realization (Chapter 7 – Part B) – ELM-806

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Certification Training

ISO 13485:2016 – Measurement Analysis and Improvement (Chapter 8 – Part A) – ELM-807

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Certification Training

ISO 13485:2016 – Measurement Analysis and Improvement (Chapter 8 – Part B) – ELM-808

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Certification Training

GMP: 21 CFR Part 820 Subpart A – General Provisions – ELM-301

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Certification Training

GMP: 21 CFR Part 820 Subpart B – Quality System Requirements (QSR) – ELM-302

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Certification Training

GMP: 21 CFR Part 820 Subpart C – Design Controls – ELM-303

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Certification Training

GMP: 21 CFR Part 820 Subpart D – Document Controls – ELM-304

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Certification Training

GMP: 21 CFR Part 820 Subpart E – Purchasing Controls – ELM-305

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Certification Training

GMP: 21 CFR Part 820 Subpart F – Identification and Traceability – ELM-306

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Certification Training

GMP: 21 CFR Part 820 Subpart G – Production and Process Controls – ELM-307

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Certification Training

GMP: 21 CFR Part 820 Subpart H – Acceptance Activities – ELM-308

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Certification Training

GMP: 21 CFR Part 820 Subpart I – Nonconforming Products – ELM-309

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Certification Training

GMP: 21 CFR Part 820 Subpart J – Corrective and Preventive Action – ELM-310

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Certification Training

GMP: 21 CFR Part 820 Subpart K – Labeling and Packaging Control – ELM-311

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Certification Training

GMP: 21 CFR Part 820 Subpart L – Handling, Storage, Distribution and Installation – ELM-312

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Certification Training

GMP: 21 CFR Part 820 Subpart M – Records – ELM-313

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Certification Training

GMP: 21 CFR Part 820 Subpart N – Servicing – ELM-314

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Certification Training

GMP: 21 CFR Part 820 Subpart O – Statistical Techniques – ELM-315

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Certification Training

Good Distribution Practices in Pharma (GDP) – Part 1 – ELM-234

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Certification Training

Good Distribution Practices in Pharma (GDP) – Part 2 – ELM-235

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Certification Training

Good Distribution Practices in Pharma (GDP) – Part 3 – ELM-240

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Certification Training

Quality Risk Management (QRM) – An Introduction to ICH Q9 – Part 1 – ELM-232a

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Certification Training

Quality Risk Management (QRM) – How QRM Applies to You and Regulations Review – Part 2 – ELM-232b

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Certification Training

EU MDR: EU Medical Device Regulation – Introduction – ELM-316

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Certification Training

EU MDR: EU Medical Device Regulation – Chapters 1 to 5 – ELM-327

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 1: Scope and Definitions – ELM-317

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 2: Making Available on the Market – ELM-318

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 3: Identification, Traceability and Registration of Devices – ELM-319

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 4: Notified Bodies – ELM-320

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 5: Classification and Conformity – ELM-321

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Certification Training

EU MDR: EU Medical Device Regulation – Chapters 6 to 10 – ELM-328

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 6: Clinical Evaluation and Clinical Investigations – ELM-322

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 7: Post Market Surveillance, Vigilance and Market Surveillance – ELM-323

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 8: Cooperation Between Member States, Medical Device Coordination Group, Expert Laboratories, etc. – ELM-324

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Certification Training

EU MDR: EU Medical Device Regulation – Chapter 9: Confidentiality, Data Protection, Funding and Penalties – ELM-325

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Certification Training

EU MDR: EU Medical Device Regulations – Chapter 10: Final Provisions – ELM-326

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Certification Training

MDSAP: Medical Device Single Audit Program – Part 1 of 3 – ELM-135

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Certification Training

MDSAP: Medical Device Single Audit Program – Part 2 of 3 – ELM-136

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Certification Training

MDSAP: Medical Device Single Audit Program – Part 3 of 3 – ELM-137

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Certification Training

MDSAP: Medical Device Single Audit Program – Chapters 1 to 4 – ELM-138

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Certification Training

MDSAP: Medical Device Single Audit Program – Chapters 5 to 7 – ELM-139

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Certification Training

MDSAP: Country Specific Requirements for USA – ELM-143

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Certification Training

MDSAP: Country Specific Requirements for Canada – ELM-142

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Certification Training

MDSAP: Country Specific Requirements for Australia – ELM-140

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Certification Training

MDSAP: Country Specific Requirements for Brazil – ELM-141

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Certification Training

MDSAP: Country Specific Requirements for Japan – ELM-144

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Certification Training

Process Validation: Introduction to Process Validation – Part 1 of 2 – ELM-401

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Certification Training

Process Validation: Introduction to Process Validation – Part 2 of 2 – ELM-402

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Certification Training

MedDev: Introduction to Medical Device Validation (Part 1 of 3) – ELM-156

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Certification Training

MedDev: Introduction to Medical Device Validation (Part 2 of 3) – ELM-157

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Certification Training

MedDev: Introduction to Medical Device Validation (Part 3 of 3) – ELM-158

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Certification Training

Validation: Introduction to Software Validation (Part 1 of 2) – ELM-113

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Certification Training

Validation: Introduction to Software Validation (Part 2 of 2) – ELM-119

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Certification Training

Validation: The Life Cycle of a Software Validation Protocol – ELM-111

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Certification Training

Validation: Implementing Compliant Systems in the Cloud – ELM-118

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Certification Training

Validation: Managing and Ensuring Data Integrity of E-Records within a Regulated Environment – ELM-125

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Certification Training

CSV: Computer System Validation – Basic Concepts & GAMP®5 – ELM-132

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Certification Training

CSV: Computer System Validation – The Regulated Software Life Cycle – ELM-133

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Certification Training

CSV: Computer System Validation – Requirements: The Basis for Validation – ELM-134

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Certification Training

CSV: Computer System Validation – Risk Management – ELM-162

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Certification Training

CSV: Computer System Validation – The Master Validation Plan (MVP) – ELM-163

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Certification Training

CSV: Application of the Validation Plan – ELM-164

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Certification Training

CSV: Validation Testing – Part 1 – ELM-165A

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Certification Training

CSV: Validation Testing – Part 2 – ELM-165B

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Certification Training

CSV: Maintaining the Validated State – ELM-166A

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Certification Training

CSV: Supplier Provided Software – ELM-166B

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Certification Training

CSV: Special Topics – ELM-167

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Certification Training

CSV: Periodic Review Strategies – Part 1 – ELM-149A

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Certification Training

CSV: Periodic Review Strategies – Part 2 – ELM-149B

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Certification Training

21 CFR Part 11 – An Introduction – ELM-112

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Certification Training

21 CFR Part 11 – Electronic Records – ELM-114

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Certification Training

21 CFR Part 11 – Electronic Signatures – ELM-115

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Certification Training

21 CFR Part 11 – 2003 Guidance – ELM-116

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Certification Training

GDocP: Good Documentation Practices and Data Integrity – ELM-104

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Certification Training

GDocP: Corrective Actions and Preventive Actions (CAPA) – Including Root Cause Analysis – ELM-117

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Certification Training

GDocP: How to Write Effective Standard Operating Procedures (SOPs) – ELM-126

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Certification Training

GDocP: How to Write an Effective Equipment User Requirement Specification (URS) – ELM-127

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Certification Training

GDocP: How to Manage Deviations in a GMP Environment – Part 1 of 2 – ELM-130

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Certification Training

GDocP: How to Manage Deviations in a GMP Environment – Part 2 of 2 – ELM-131

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Certification Training

GDocP: Good Documentation Practices – General Rules of Data Integrity – ELM-501

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Certification Training

GDocP: Good Documentation Practices – Making Correction to Ensure Data Integrity – ELM-502

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Certification Training

GDocP: Good Documentation Practices – Logbook Data Integrity – ELM-503

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Certification Training

GDocP: Good Documentation Practices – Data Integrity for General Test Results – ELM-504

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Certification Training

Data Integrity: An Introduction to Data Integrity – ELM-148

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Certification Training

Data Integrity: Health Authority Expectations – ELM-151

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Certification Training

Data Integrity: ALCOA and ALCOA+ – ELM-152

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Certification Training

Data Integrity: Good Documentation Practice (GDocP) – ELM-153

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Certification Training

Data Integrity: Computer System Validation (CSV) Best Practices – ELM-154

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Certification Training

Data Integrity: Data Governance – ELM-155

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Certification Training

Equipment Validation: How to Perform Supplier Qualification – ELM-107

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Certification Training

Equipment Validation: Introduction to Risk Based Equipment Qualification – ELM-121

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Certification Training

Equipment Validation: How to Perform a Failure Mode Effect Analysis (FMEA) – Part 1 – ELM-128

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Certification Training

Equipment Validation: How to Perform a Failure Mode Effect Analysis (FMEA) – Part 2 – ELM-129

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Certification Training

Commissioning, Qualification & Validation: The Concept of CQV – Part 1 – ELM-181

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Certification Training

Commissioning, Qualification & Validation: The Concept of CQV – Part 2 – ELM-182

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Certification Training

Commissioning, Qualification & Validation: The Concept of CQV – Part 3 – ELM-183

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Certification Training

Change Control – Regulations & Guidelines – ELM-159

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Certification Training

Change Control & Change Management – ELM-160

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Certification Training

The Lifecycle of a Change Control Program – Phase 1: Develop the Change Request – ELM-161

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Certification Training

The Lifecycle of a Change Control Program – Phase 2: Evaluate – ELM-178

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Professional Designation in Clinical Trials Management – GCP00S1

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Glaucoma: Treatment – GLAUT

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Heart Failure: Four Course Suite – HEFAS

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HIV and AIDS: Diagnosis – HIVAD

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HIV and other Viral Infections: Five Course Suite – HIVAS

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Human Gene Therapy – HUGET

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Medical Device Regulatory Affairs: Australian Overview – MDA1

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Myocardial Infarction: Diagnosis – MYIND

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Myocardial Infarction: Three Course Suite – MYINS

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Myocardial Infarction: Treatment – MYINT

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Non-Hodgkin`s Lymphoma: Three-Course Suite – NHLMS

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Non-Hodgkin`s Lymphoma: Treatment – NHLMT

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Nociceptive Pain: Cause – NNPAC

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Nociceptive Pain: Diagnosis – NNPAD

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Nociceptive Pain: Three Course Suite – NNPAS

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Nociceptive Pain: Treatment – NNPAT

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Central Nervous System: Histology – NSAPH

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Central Nervous System: Neuroanatomy – NSAPN

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Central Nervous System Anatomy and Physiology: Two Course Suite – NSAPS

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Non-Small Cell Lung Cancer: Cause – NSCLC

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Non-Small Cell Lung Cancer: Diagnosis – NSCLD

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Non-small Cell Lung Cancer (NSCLC): Three Course Suite – NSCLS

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Non-Small Cell Lung Cancer: Treatment – NSCLT

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Certification Training

Overactive Bladder (OAB): Cause – OABLC

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Overactive Bladder (OAB): Diagnosis – OABLD

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Overactive Bladder (OAB): Three Course Suite – OABLS

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Overactive Bladder (OAB): Treatment – OABLT

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Certification Training

On Demand Training 10000 (10% Discount) – OD10000

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On Demand Training 2500 (5.0% Discount) – OD2500

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On Demand Training 5000 (7.5% Discount) – OD5000

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Certification Training

Osteoarthritis: Cause – OSARC

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Osteoarthritis: Diagnosis – OSARD

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Osteoarthritis: Three Course Suite – OSARS

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Osteoarthritis: Treatment – OSART

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Pancreatic Cancer: Cause – PANCC

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Pancreatic Cancer: Diagnosis – PANCD

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Pancreatic Cancer: Three Course Suite – PANCS

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Pancreatic Cancer: Treatment – PANCT

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Password Reset – PASS01

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The PhRMA Code – PHRMP

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Professional Designation in US Pharmaceutical Regulatory Affairs – PRA000S1

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Pharmaceutical Regulatory Affairs: Essentials for Human Medicinal Products – EU and US – PRA001

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Pharmaceutical Regulatory Affairs: Orphan Drug Application – EU and US – PRA002

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Pharmaceutical Regulatory Affairs: Preparing Submissions in the Common Technical Document (CTD) Form – PRA003

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Pharmaceutical Regulatory Affairs: Electronic Common Technical Document (eCTD) – PRA004

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Regulatory Affairs: Registration of Drugs Based on Monoclonal Antibodies – PRA005

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Pharmaceutical Regulatory Affairs: The ANDA: Requirements for Obtaining FDA Approval for a Generic Product in the USA – PRA006

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Pharmaceutical Regulatory Affairs: The NDA Process: Requirements for Obtaining Approval for a New Drug in the USA – PRA007

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Regulatory Affairs for Monoclonal Antibodies Professional Certification Program – PRA00A2

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Pharmaceutical Regulatory Affairs: The European Centralized Procedure (CP) – PRA020

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Pharmaceutical Regulatory Affairs: The Mutual Recognition Procedure (MRP) – PRA021

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Pharmaceutical Regulatory Affairs: EU Variations Procedure – PRA022

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Pharmaceutical Regulatory Affairs: The Decentralized Procedure (DCP) – PRA023

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Certification Training

Prostate Cancer: Cause – PRCAC

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Prostate Cancer: Diagnosis – PRCAD

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Prostate Cancer: Three Course Suite – PRCAS

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Prostate Cancer: Treatment – PRCAT

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Proteomics – PROTE

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Rheumatoid Arthritis: Cause – RHARC

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Rheumatoid Arthritis: Diagnosis – RHARD

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Rheumatoid Arthritis: Three Course Suite – RHARS

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Rheumatoid Arthritis: Treatment – RHART

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Rhinitis: Cause – RHINC

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Rhinitis: Diagnosis – RHIND

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Rhinitis: Three-Course Suite – RHINS

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Rhinitis: Treatment – RHINT

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Respiratory System: Anatomy – RSAPA

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Respiratory System: Physiology – RSAPP

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Respiratory System Anatomy and Physiology: Two Course Suite – RSAPS

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Schizophrenia: Cause – SCHIC

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Schizophrenia: Diagnosis – SCHID

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Schizophrenia: Three Course Suite – SCHIS

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Schizophrenia: Treatment – SCHIT

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Small Cell Lung Cancer: Cause – SCLCC

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Small Cell Lung Cancer: Diagnosis – SCLCD

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Small Cell Lung Cancer (SCLC): Three Course Suite – SCLCS

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Small Cell Lung Cancer: Treatment – SCLCT

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Sepsis: Cause and Identification – SEPCI

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Sepsis: Two Course Suite – SEPSS

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Sepsis: Treatment – SEPST

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SNPs: Identification and Uses – SNPIU

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Certification Training

Social Media for Healthcare Overview: Essentials and legal concerns – SOME001

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Mega-Conversions for your Website: How to design and manage your online community for better reputation management and profit – SOME002

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Dominating Twitter: How to engage people and build a massive following in 30 days – SOME003

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Dominating LinkedIn: How to engage people and build trust in 30 days – SOME004

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Blogging for Healthcare: How to create a successful blog, even if you’re not a writer! – SOME005

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Accentuate the Positive! How to make a Healthcare Listening Dashboard – SOME006

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Quickly Creating Relationships online: How to engage people, market your business and build trust in 15 minutes a day – SOME007

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Awesome Healthcare marketing policies: Putting it all together – SOME008

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Social Media for Healthcare Professional Certification Program – SOMEA01

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Social Media for Healthcare: Digital Marketing 101 – SOMEF01

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Stroke: Cause – STROC

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Stroke: Diagnosis – STROD

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Stroke: Three Course Suite – STROS

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Stroke: Treatment – STROT

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Thrombosis and Thromboembolism: Cause – THRTC

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Thrombosis and Thromboembolism: Diagnosis – THRTD

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Thrombosis and Thromboembolism: Three Course Suite – THRTS

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Thrombosis and Thromboembolism: Treatment – THRTT

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Type 2 Diabetes: Cause – TY2DC

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Type 2 Diabetes: Diagnosis – TY2DD

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Type 2 Diabetes: Three Course Suite – TY2DS

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Type 2 Diabetes: Treatment – TY2DT

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Certification Training

Ulcerative Colitis: Cause – ULCOC

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Ulcerative Colitis: Diagnosis – ULCOD

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Ulcerative Colitis: Three Course Suite – ULCOS

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Ulcerative Colitis: Treatment – ULCOT

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Upper GI Cancer: Cause – UPGIC

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Upper GI Cancer: Diagnosis – UPGID

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Upper GI Cancer: Three Course Suite – UPGIS

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Upper GI Cancer: Treatment – UPGIT

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Valvular Disease: Cause – VALDC

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Valvular Disease: Diagnosis – VALDD

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Valvular Disease: Three Course Suite – VALDS

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Valvular Disease: Treatment – VALDT

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Certification Training

Anatomy of the Cardiovascular System – VSAPA

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Physiology of the Cardiovascular System – VSAPP

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Renal System – VSAPR

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Cardiovascular System Anatomy and Physiology: Three Course Suite – VSAPS

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For quotes or invoices please provide the course(s) and number of students.