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Home » GMP: Proper Documentation Practices

GMP: Proper Documentation Practices (EGMPSP02)

Certification Training
Rated 3.67/5
3 reviews
Method of Training: Online / Self-paced eLearning.
Credit Hours: 1 credits.
Duration: ~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

BioPharma Institute LogoTraining Program: GMP: Proper Documentation Practices
Training Provided By: BioPharma Institute

Schedule: Self-paced. Immediate access to training materials upon ordering.

Description: Online training with immediate access upon enrollment. BioPharma Institute Reviews

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 a review of the proper way to input information into GMP documents, how to correct mistakes found in documents, and other acceptable documentation practices. The GMP proper documentation practices course is suitable for new employees and individuals who are required by their companies to undergo a refresher course, or as part of preventive action for documentation deviation. One needs to achieve an 80% passing grade for successful course completion and to launch the certificate of completion.

Benefits of Getting Certified at BioPharma Institute

At the BioPharma Institute, providing education for your employees and maintaining their training records has never been easier. Whether you are using BioPharma Institute online training solutions as an employee or individual, you will have access to high quality learning tools such as, HD animations, progress checks, and voice-overs. You can rest assured that our course content is easy to digest and you can grasp many different learning concepts in no time. We have been providing comprehensive and flexible online learning solutions since 1997, and our courses are recognized across a wide range of healthcare, pharmaceutical, and biotechnology industries.

Have Questions?

Should you have any particular question about this course, you can call us at (888) 424-6576 or send us an email at for more information.

Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with passing score within a 90-day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.

The GMP: Proper Documentation Practices course is found in the following professional certification program(s):

cGMP for Medical Devices Professional Certification Program: This program is essential for those to learn how to be compliant with the FDA's quality system regulations for current good manufacturing practices (cGMP), with emphasis on medical devices. This certification p ... Learn more


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

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