100%
Home
eLearning Courses
All Courses
View All Courses
Medical Device Courses
Pharma/Biopharma Courses
Combination Product Courses
Problem Solving Courses
Sectors
Staff Training Needs
Training for MedTech Manufacturing Startups
Drug/Device Combination Products
Upskill/Reskill for work in MedTech
In-Company Training
Medical Devices
Medical Device Micro-Training Courses
Quality Systems
ISO 13485:2016 Clause by Clause
Introduction to 21 CFR 820 Quality System
CAPA
CAPA in the Medical Device Industry
Project Management Skills for an Effective CAPA
Audit preparation
How to Prepare for a FDA QSIT Inspection
How to Prepare for a Medical Device Single Audit Program (MDSAP)
Combination Products
Annual cGMP Drug/Device Combination Products (21 CFR 820, ISO 13485:2016, CFR Part 4, 210 and 211)
Pharma/Biopharma
Pharma/Biopharma Industries Micro-Training Courses
CGMP Essentials for the Pharma/Biopharma industry
Quality Management
Quality Management Systems
ISO 9001:2015 Clause by Clause Classroom Training
Quality Culture
Creating a Quality Culture
Problem Solving
A3 Problem Solving Training Course
Food Safety Management
Introduction to HACCP Classroom Training
ISO 22000 Clause by Clause Classroom Training
Soft Skills
Effective Meeting Skills Classroom Training
Lean Management
5S Training Course
Mistake Proofing (Poka Yoke) Training
Core Tools
Failure Mode and Effect Analysis (FMEA)
Effective Technical Writing Skills
Virtual Training
Medical Devices
Internal Auditor ISO 13485:2016 Training Course
Introduction to CAPA for Medical Devices Training Course
Introduction to ISO 13485:2016 Training Course
EU Medical Device Regulation (MDR) 2017/745 Fundamentals Training Course
Quality Management Systems
Internal Auditor ISO 9001:2015 Training Course
Introduction to ISO 9001:2015 Training Course
Food Safety Management (HACCP)
HACCP Food Safety Management Fundamentals Training Course
Resources
Blog
Glossary
FREE Micro-Learning Videos
Useful Links
FAQ
eLearning FAQ
About us
Contact Us
Login
Home
eLearning Courses
In-Company Training
Virtual Training
Resources
FAQ
About us
Contact Us
All Courses
Sectors
View All Courses
Medical Device Courses
Pharma/Biopharma Courses
Combination Product Courses
Problem Solving Courses
Staff Training Needs
Training for MedTech Manufacturing Startups
Drug/Device Combination Products
Upskill/Reskill for work in MedTech
Medical Devices
Combination Products
Pharma/Biopharma
Quality Management
Food Safety Management
Soft Skills
Lean Management
Core Tools
Medical Device Micro-Training Courses
Quality Systems
CAPA
Audit preparation
ISO 13485:2016 Clause by Clause
Introduction to 21 CFR 820 Quality System
CAPA in the Medical Device Industry
Project Management Skills for an Effective CAPA
How to Prepare for a FDA QSIT Inspection
How to Prepare for a Medical Device Single Audit Program (MDSAP)
Annual cGMP Drug/Device Combination Products (21 CFR 820, ISO 13485:2016, CFR Part 4, 210 and 211)
Pharma/Biopharma Industries Micro-Training Courses
CGMP Essentials for the Pharma/Biopharma industry
Quality Management Systems
Quality Culture
Problem Solving
ISO 9001:2015 Clause by Clause Classroom Training
Creating a Quality Culture
A3 Problem Solving Training Course
Introduction to HACCP Classroom Training
ISO 22000 Clause by Clause Classroom Training
Effective Meeting Skills Classroom Training
5S Training Course
Mistake Proofing (Poka Yoke) Training
Failure Mode and Effect Analysis (FMEA)
Effective Technical Writing Skills
Medical Devices
Quality Management Systems
Food Safety Management (HACCP)
Internal Auditor ISO 13485:2016 Training Course
Introduction to CAPA for Medical Devices Training Course
Introduction to ISO 13485:2016 Training Course
EU Medical Device Regulation (MDR) 2017/745 Fundamentals Training Course
Internal Auditor ISO 9001:2015 Training Course
Introduction to ISO 9001:2015 Training Course
HACCP Food Safety Management Fundamentals Training Course
Blog
Glossary
FREE Micro-Learning Videos
Useful Links
eLearning FAQ
Home
/
Uncategorized
/ 21 CFR Part 211 Subpart E – Control of Components and Drug Product Containers and Closures Online Training Course
21 CFR Part 211 Subpart E – Control of Components and Drug Product Containers and Closures Online Training Course
Price:
€
215.00
Add to Cart
BUY NOW
Related Products
21 CFR 210 / 211 CGMP’s for Finished Pharmaceuticals Online Training Course
€
1,295.00
21 CFR Part 4 (Subpart A) – cGMP for Combination Products Online Training Course
€
295.00
Introduction to FDA cGMP Requirements for Drug/Device Combination Products Online Training Course
€
395.00
Affinity Analysis Technique Online Training Course
€
125.00
