Length of Course: Approximate time to complete this course is 1 hour(s).
Self-paced Training: 24/7 access to course.
Enrollment Period: 3 months.
Catalog: Good Manufacturing Practices (GMP).
Demonstration: Try one of our FREE courses.
Certificate: View sample certificate.
PRICE: USD $95.00
Training Program: 21 CFR Part 820: cGMP System Regulation
Training Provided By: BioPharma Institute
Availability: Immediately available upon ordering.
Description: Online training with immediate access upon enrollment.
The 21 CFR Part 820: cGMP System Regulation course summarizes the essential elements of cGMP regulations governing the methods and facilities used for the servicing, installation, storage, labeling, packaging, manufacture, and design of finished medical devices intended for human use. The course is part of the Employee cGMP for Medical Devices Professional Certification Program and serves as a stellar refresher for seasoned employees. Students will be able to view interesting and informational content, such as a live action video from a real medical device company. At the end of the course, student will take an online, multiple-choice final assessment where an 80% or better score is required to launch the certificate of completion.
Benefits of Getting Certified at BioPharma Institute
BioPharma Institute is a training organization which pharmaceutical, biotechnology, and healthcare professionals can rely on for online training programs. Whether you are looking to upgrade your skills, or to have a refresh for your knowledge on certain topics, you will find our online learning solutions most effective, flexible, and comprehensive. Our Institute was founded in 1997, and we have had many years of experience in helping small businesses and large corporations train their employees.
When you use our eLearning system, you automatically gain access to an array of easy to use tools like voice-overs, automated tracking systems, high quality animations, and books. As our course content are extremely easy to digest, you will be able to understand different learning concepts adequately.
Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with >80% passing grade within a 90 day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.
The 21 CFR Part 820: cGMP System Regulation course is found in the following professional certification program(s):
Outline is not currently available, online. If you would like an outline of this training program, complete the Contact Us form at the bottom of this page.
The objective for this training is to provide the learner with a deeper knowledge within this subject matter.
All Courses in the GMP Employee Training Catalog:
|21 CFR Part 211: cGMP Regulations and Controls: The 21 CFR Part 211: cGMP Regulations and Controls training course is one of six training content sections covered under the 21 CFR Part 211 Employee Certification Program. When it comes to designing, manufactu ... Learn more|
|21 CFR Part 211 Subpart B: Organization and Personnel: The organization and personnel (21 CFR Part 211, Subpart B) training course is one of the six courses that make up the 21 CFR PART 211 Employee Certification Program. As an employee working in a pharmaceutical ... Learn more|
|21 CFR Part 211 Subpart C: Buildings and Facilities: This buildings and facilities course (21 CFR Part 211 Subpart C) is one of the courses covered in the 21 CFR PART 211 Employee Certification Program. Students will gain an in-depth understanding of the requirem ... Learn more|
|21 CFR Part 211 Subpart D: Equipment: The 21 CFR Part 211 Subpart D, Equipment Course discusses both the design and construction requirements for lubrication and coolants, documentation requirements, personnel training requirements, equipment ident ... Learn more|
|21 CFR Part 211 Subpart E: Materials: The 21 CFR Part 211 Subpart E: Materials Course is one part of the 21 CFR PART 211 Employee Certification Program. The course consists of topics that cover GMP requirements, such as supplier qualification, manu ... Learn more|
|21 CFR Part 211 Subpart F: Production and Process Controls: The 21 CFR Part 211 Subpart F: Production and Process Controls course reviews the requirements which need to be met to assure drug products have the purity, quality, strength, and identity they are represented ... Learn more|
|GMP: Contamination Control for Employees: The GMP: Contamination Control for Employees course covers topics such as potential sources of contamination and ways to prevent medical products from becoming contaminated. The course is also included in the E ... Learn more|
|GMP: Proper Documentation Practices: The GMP - Proper Documentation Practices course is one of the courses found in the Employee cGMP for Medical Devices Professional Certification Program. The course consists of various topics. The topics include ... Learn more|
|GMP: Root Cause Analysis: The GMP - Root Cause Analysis Course provides answers on how clinical, pharmaceutical, and laboratory professionals can investigate, identify, and resolve root cause of deviations in modern manufacturing practi ... Learn more|
|21 CFR Part 820: cGMP System Regulation: The 21 CFR Part 820: cGMP System Regulation course summarizes the essential elements of cGMP regulations governing the methods and facilities used for the servicing, installation, storage, labeling, packaging, ... Learn more|
|GMP: Surviving an FDA Inspection: This GMP - Surviving an FDA Inspection Program teaches participants how to behave during, how to plan for, and what to expect from an inspection. This program has demonstrations involving different response str ... Learn more|
|GMP: Understanding Validation: This GMP - Understanding Validation program provides a overview of good manufacturing practice, with a comprehensive emphasis to understanding validation. This course, which is based on a 2008 guidance document ... Learn more|
Online Training: The Benefits of eLearning
- Immediate access to training: Instructions, username, password and receipt of payment emailed instantly upon online enrollment
- Optimized for learning: Courses include voice-overs, easy navigation, progress checks, and high-quality animations to increase retention of subject matter
- Self-paced courses: 24/7 access to individual courses for 90 days; and 180 days for professional certification programs
- Flexible final assessments: Tests include multiple-choice questions and can be taken repeatedly until a passing score is achieved
- Direct access to certificates: Documentation instantly available once course requirements have been fulfilled
- Verification of training: Certificates can be verified online, and electronic badges are issued for all Professional Certification programs
- Tuition reimbursement: Some employers may reimburse for training expenses; check on your company's requirements
- Purchase orders (POs) accepted: If POs are required, request an invoice to start the procurement process
- Corporate LMS compatibility: All courses are SCORM compliant and can be delivered from most corporate Learning Management Systems
- Secure and safe access: Website and LMS offer an encrypted connection with firewall protection and daily scans for optimal level of security and performance
- Career advancement: Professional certifications could be helpful for those seeking new careers or transitioning to different positions within their organization
For more information on the BioPharma Institute's training programs, or to suggest a course, please complete the form located below. Alternatively, you may call toll free in the US: (888) 4-BIO-LRN, international callers can dial (201) 301-8370, or email Support@BioPharmaInstitute.com.