A Comprehensive Overview of Good Documentation Practices and Record Keeping in the US and Europe

$799.00

ID:           938
SKU:       IC-0001-BP
Type:      In-Class Course

 

This one day On-in-class course covers the essentials of GDP, its definition, purpose, and importance. Then expands on general rules and principles of GDP (US & EU), GDP as applies to laboratory notebook (paper and electronic) documentation, and GMP on non-clinical laboratory studies (21 CFR Part 58), document and record keeping best practices specifically as it applies to drugs and devices (21 CFR Parts 212, 211, 312, and 812), USP General Chapter <1029>, Rules Governing Medicinal Products in the European Union (Vol. 4: Documentation),  and finally discussing GDP enforcement by regulatory bodies in different countries with some examples of FDA citations.


SKU: IC-0001-BP

Category:

Description

Speaker Bio

 

Dr. Afsaneh Motamed Khorasani is a Medical and scientific Affairs expert and a Senior Scientist with a strong background in biomedical science and clinical trial/research. She has a tenured and diverse range of experience in medical affairs, basic and industrial clinical research and development, clinical trials, Medical and regulatory writing and intellectual property. She is currently the Vice President of Medical Affairs at Easy Global Training, which is a US-based firm providing global regulatory, quality and medical affairs training backed by consulting. Before joining this company, Dr. Motamed Khorasani has served as an independent consultant, director of medical affairs, senior medical sciences liaison, senior scientist and senior medical analyst at Merck (MDS), Johnson & Johnson, United States Pharmacopoeia Convention (USP), Amgen, Baxter International, Covidien (eV3), Radient Pharmaceuticals, AMDL Diagnostics, Microbix Biosystems, Neometrix Consulting, Mount Sinai Hospital, Princess Margaret Hospital, and Vancouver General Hospital. She has more than 20 years of experience and many National and international certificates in GLP, GMP, ICH-GCP and global regulatory compliance for clinical trials and is a member in a number of professional associations, including: American Association of Cancer Research (AACR), American Medical Writers Association (AMWA), Regulatory Affairs Professional Society (RAPS), American Society of Quality (ASQ), Project Management Institute (PMI), and Intellectual Property Institute of Canada (IPIC). Dr. Motamed Khorasani’s research has focused on high throughput approaches in the context of cancer informatics with a particular interest in the use of comparative analysis for the mining of integrated oncology data sets that include protein-protein interaction and gene expression profiling. She has published and presented more than 50 papers, abstracts and articles in highly regarded scientific journals and high profile conferences and scientific meetings.

Course Overview

Good documentation Practices (GDP) is an essential factor that needs to be closely followed by the personnel in any regulated environment as a process for a successful project completion including observations of unanticipated responses that are required to be accurately recorded and verified. This one day On-in-class course covers the essentials of GDP, its definition, purpose, and importance. Then expands on general rules and principles of GDP (US & EU), GDP as applies to laboratory notebook (paper and electronic) documentation, and GMP on non-clinical laboratory studies (21 CFR Part 58), document and record keeping best practices specifically as it applies to drugs and devices (21 CFR Parts 212, 211, 312, and 812), USP General Chapter <1029>, Rules Governing Medicinal Products in the European Union (Vol. 4: Documentation),  and finally discussing GDP enforcement by regulatory bodies in different countries with some examples of FDA citations.

Learning Highlights

  • Following the completion of this One day In-Class session you will gain an advanced knowledge of definition, purpose, importance of GDP, General rules of GDP (US / EU), GDP as applies to laboratory notebook (paper and electronic) documentation, and GMP on non-clinical laboratory studies (21 CFR Part 58), document and record keeping best practices specifically as it applies to drugs and devices (21 CFR Parts 212, 211, 312, and 812), USP General Chapter <1029>, Rules Governing Medicinal Products in the European Union (Vol. 4: Documentation), and finally discussing GDP enforcement by regulatory bodies in different countries with some examples of FDA citations.
  • The outline of this one day In-Class course includes:
    • Definition, Purpose, and Importance
    • General Rules and Principles of GDP
      • Requirements of Records
      • General Tips in GDP:
        • Signature / initial and the meaning
      • Copying records
      • Document maintenance
      • Recording the time and date
      • Correction of errors
      • Rounding rules
      • Back dating
      • Missing data
      • Voiding / cancelling records
      • Recreating / rewriting records
      • Deviations
    • General Tips for Laboratory Notebook Documentation:
      • Assignment of Lab notebook
      • How to properly document in lab notebooks
      • How to include tables / graphs
      • How to attach instrument print outs
      • How to include metadata
      • How to reference lab notebook
      • How to store the completed lab notebooks
    • Non-clinical laboratory studies (21 CFR Part 58)
    • Documentation / record keeping best practices as it applies to drugs (21 CFR Parts 212, 211, 312)
    • Documentation / record keeping best practices as it applies to devices (21 CFR Parts 812)
    • US Pharmacopoeia General Chapter <1029>
    • Rules Governing Medicinal Products in the European Union (Vol. 4: Documentation)
      • What is new in the Latest Version?
      • Outline of EU GDP Regulations
    • GDP Enforcement plus Excerpts of FDA observations
    • Summary
    • References
Who Can Benefit From This Course
  • Anybody who works in a regulated environment
  • Manufacturing & Production Personnel / Managers
  • Research and Development Personnel (R&D) / Managers
  • Quality Assurance & Quality Control Personnel / Managers
  • Laboratory Personnel / Managers
  • Validation Specialists
  • Clinical trial personnel
  • Project Managers
Details
  • ID:                                     938
  • SKU:                                 IC-0001-BP
  • Type:                                In-Class Course
  • Format:                            PDF Hand Outs
  • Date of Last Update:     Feb 23, 2017
  • Duration:                         1 Day
  • Price:                               $799.00
Notes

For all the In-Class Courses, please contact us at info@easyglobaltraining.com for request and registrations. The In-Class courses are held only in response to requests made or upon invitation to your site for and On-Site Training for your company