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Good Laboratory Practice (GLP)

Good Laboratory Practice (GLP) Certification Training

 
Rated 4.2 / 5
(17 reviews)

Program/Course ID:GLP01
Enrollment Period:12 months.
Average Learning Time:~60 minutes.
Additional Resources:Supplemental materials & activities.
Accredited Program:1 CPD Credits.
Method of Training:
Self-paced, online, asynchronous eLearning.
Accessibility:24/7 access to all program materials.
Catalog:Good Laboratory Practices.
Demonstration:Four (4) free trial courses are available.
Group/Employee Training: Click here to request a quote or invoice.
Final Assessment:Multiple choice; unlimited attempts.
Certificate:Encrypted PDF with QR validation code.
  Price: $199.00 USD  
CPD Accredited Training

Showcase your commitment to quality, compliance, safety, and professional excellence by earning a recognized certification of training.

Training Program: Good Laboratory Practice (GLP)
Training Provided By: Biopharma Institute
Website: https://www.biopharmainstitute.com

Schedule: Self-paced eLearning. Immediate access to training materials upon enrollment.
Description:
Biopharma Institute Reviews

Elevate your professional expertise with our Good Laboratory Practice (GLP) training - the gold standard for ensuring the quality, integrity, and reliability of nonclinical study data. Whether you are entering the field or refreshing your knowledge, this program equips you with the essential skills to confidently meet global regulatory requirements.

GLP standards are the backbone of credible scientific research, governing the planning, performance, monitoring, recording, and reporting of studies. Regulatory authorities worldwide require strict adherence to GLP for nonclinical studies supporting applications for clinical research or product marketing approval. This course ensures you know exactly how to meet these standards - and avoid costly noncompliance penalties.

In this program, you will:

  • Discover the history and evolution of GLP and why it remains critical today
  • Understand global regulatory expectations and their application in real-world studies
  • Identify penalties and consequences of noncompliance - and how to avoid them
  • Gain insight into the two main sources of GLP rules:
    • OECD Principles on Good Laboratory Practice
    • US 21 CFR Part 58: Good Laboratory Practice for Nonclinical Laboratory Studies
  • Learn best practices to ensure data credibility, regulatory readiness, and study reproducibility

Why enroll in this program?

  • Stay compliant with global GLP regulations
  • Enhance your career opportunities in pharmaceuticals, biotechnology, and research
  • Build confidence in managing studies that pass regulatory inspections with ease
  • Acquire a recognized professional credential from an industry-trusted provider

Whether your goal is to deepen your understanding, strengthen compliance, or advance your career, this GLP training provides the knowledge and confidence to excel in nonclinical research environments worldwide.

Take the next step in your professional growth and earn an industry-recognized certification from Biopharma Institute -designed for professionals who want to excel in ensuring the safety and effectiveness of medicinal products.

These programs not only give you up-to-date regulatory and compliance insights but also deliver practical skills that employers value. Whether you're enhancing your current role or preparing for a new opportunity, Biopharma Institute certifications are designed to set you apart in the competitive and highly regulated pharmaceutical industry.


Outline:


History and purpose of GLP:
The purpose of GLP in providing assurance of the integrity of nonclinical data. The development and application of the US GLP Regulation and the OECD Principles of GLP. Consequences of failure to comply with GLP.

Test facility organization and personnel:
Responsibilities, under GLP, of test facility management, the study director, laboratory personnel, and the quality assurance unit/program.

Planning and performance of studies:
GLP requirements for laboratory facilities, equipment, SOPs, care of animals and other test systems, test and reference items / test and control articles, study plans/protocols, and study conduct.

Study reporting and post-study considerations:
GLP requirements for reporting of study results and for storage and retention of records and materials. Regulatory inspection of test facilities.

Level: Introductory, Intermediate.
Region: USA, Europe, Other.

Objectives:


This module provides essential learning for all personnel of analytical laboratories, especially those working in test facilities undertaking nonclinical studies.

Learning Objectives:
Explain the purpose of Good Laboratory Practice (GLP) and describe the development of the US GLP Regulation and the OECD Principles of GLP

Identify consequences of failure to comply with GLP

Specify GLP requirements for laboratory organization and the responsibilities of personnel

Specify GLP requirements for the planning and performance of studies

Specify GLP requirements for reporting of study results and the storage and retention of records and materials

Identify typical findings of regulatory inspections of laboratories

Related Professional Certification Programs:


Professional Certification Program:

Good Laboratory Practice (GLP) Professional Certification Program

Program ID: GLPRO
Price: $1295.00 (USD)

Certification Requirements: To earn a certificate, students must complete the entire course and pass an online, multiple-choice final assessment within 12 months of enrollment. Upon meeting these requirements, a certificate of completion is instantly available in PDF format.

Biopharma Institute's online training provides immediate access after enrollment. Students receive their username, password, and instructions via email directly after registering. The final assessment can be attempted as many times as necessary to achieve a passing score. Once the course is successfully completed, the certificate is generated instantly in an encrypted PDF format, featuring a watermark, unique validation code, and QR verification barcode.

Training achievements can be verified on our website using the certificate's unique ID or QR code. For professional certification programs, a digital badge is also issued, allowing students to showcase their accomplishment on platforms such as LinkedIn, Facebook, Twitter, and Badgr.

Certificates and digital badges include the completion date but do not display an expiration date. Compliance training is generally considered valid for up to three years, and many organizations schedule refresher training every one to three years to maintain alignment with evolving regulations, standards, and GxP expectations. Biopharma Institute does not assign a universal expiration date as it recognizes that the validity period or recertification interval for each individual worker should be determined by each individual organization's quality management team.

Benefits of Being Certified by Biopharma Institute Our training engages students in active learning through interactive eLearning modules that are validated by independent third-party organizations for relevance, compliance, and regulatory accuracy. Each course is developed by subject matter experts (SMEs) in collaboration with instructional design professionals to maximize knowledge retention. Programs include access to regulatory references, real-life case studies, and other essential resources to support learning.

Since 2003, Biopharma Institute has helped professionals and their employers meet training requirements. Our certifications are recognized by a wide range of industries, regulatory bodies, and organizations worldwide. Training solutions can be customized to meet the needs of any organization. We currently offer over 300 courses covering topics such as clinical research, drug manufacturing (cGMP), regulatory affairs, validation systems, pharmacovigilance, good laboratory practice (GLP), and data integrity, serving the clinical research, pharmaceutical, and medical device sectors.

Employee / Corporate Training For organizations seeking a cost-effective way to train employees without the need for travel, webinars, or in-person sessions, Biopharma Institute is a trusted partner. Our programs deliver effective, engaging, self-paced learning that fits seamlessly into employees' daily routines. All eLearning modules are SCORM-compliant and can be integrated into most corporate learning management systems (LMS).

We support both small- and large-scale training initiatives, always with the same goal- providing a positive, streamlined experience for everyone involved, from students to training managers.


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Benefits of Training with Biopharma Institute

Immediate Course Access: Login details, instructions, and payment confirmation are emailed immediately upon online enrollment.
Self-Paced eLearning: Enjoy 24/7 access to all course materials and assessments for 12 months.
Open Enrollment: No prerequisites or prior work experience required to start.
Expert-Developed Content: Courses are designed by subject matter experts (SMEs) in their respective fields.
Up-to-Date & Validated: Training is regularly updated to meet current regulations and is third-party validated or accredited.
Optimized for Learning: Courses feature voiceovers, intuitive navigation, reading materials, case studies, progress checks, and animations to boost knowledge retention.
Secure Access: Encrypted connections, firewalls, and daily malware scans ensure security and system performance.
Flexible Assessments: Multiple-choice exams can be retaken until a passing score is achieved.
Instant Certificates: Certificates are issued instantly in secure PDF format with watermark, unique validation code, and QR code for verification.
Training Verification: Certificates can be verified online using a QR code or unique ID. Digital badges are included with professional certifications.
Manager Access: A secure portal allows managers to view and download enrollment reports, training records, account balances, and more.
SCORM-Compliant: Courses can be integrated directly into most corporate Learning Management Systems (LMS).
Purchase Orders: We accept POs from all companies. Request an invoice to start the procurement process.
Employer Reimbursement: Some employers may cover training costs -check your company's reimbursement policy.
Financial Assistance: Payment plans are available for eligible learners, or purchase courses individually as needed.
Career Advancement: Professional certifications highlight dedication to career growth, enhance resumes, provide interview talking points, and equip learners with practical job skills.


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