Good Documentation Practice and Record Keeping Regulations (FDA and EMA)
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Speaker : AFSANEH MOTAMED KHORASANI
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When : Thursday, October 17, 2024
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Time : 01 : 00 PM EST
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Dr. Afsaneh Motamed Khorasani, PhD, 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 AztraZeneca (AZ), Insmed, Merck (MDS), Johnson & Johnson, United States Pharmacopeia Convention (USP), Amgen, Baxter International, MedTronic, AMDL Diagnostics, Microbix Biosystems, 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), and Project Management Institute (PMI). 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 datasets that include protein-protein interaction and gene expression profiling. She is a well-published author with books, book chapters, e-books, online scientific articles, and has published and presented more than 50 papers, abstracts and articles in highly regarded scientific journals and high profile conferences and scientific meetings.
Good documentation Practices (GDP) are an essential factor that needs to be closely followed by the personnel in any regulated environment as a process for successful project completion including observations of unanticipated responses that are required to be accurately recorded and verified. This 60-min Webinar covers the essentials of GDP, its definition, purpose, and importance. Then expands on general rules and principles of GDP (US & EU), General tips for Laboratory Notebook documentation, and finally discusses GDP enforcement by regulatory bodies in different countries with some examples of FDA citations.
Areas Covered
Following the completion of this webinar you will gain a basic to moderate knowledge of the definition, purpose, and importance of GDP, General rules of GDP, GDP as applies to laboratory notebook documentation, US Pharmacopeia General Chapter <1029> introduction “Good Documentation Guidelines”, A very brief introduction to European Union (EU) GDP, and finally its enforcement along with some observation samples from FDA.
The outline of this 60 minute Webinar includes:
- Definition, Purpose, and Importance
- General Rules and Principles of GDP
o Requirements of Records
o 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 / canceling records
- Recreating/rewriting records
- Deviations - Rules Governing Medicinal Products in the European Union (Vol. 4: Documentation)
- What is new in the Latest Version? - GDP Enforcement (examples from FDA warning letters)
Course Level - Intermediate
Who Should Attend
- Anybody who works in a regulated environment
- Manufacturing & Production Personnel / Manager
- Research and Development Personnel (R&D) / Managers
- Quality Assurance & Quality Control Personnel / Managers
- Laboratory Personnel / Managers
- Validation Specialists
- Clinical trial personnel
- Project Managers
Why Should You Attend
If you are involved in any product manufacturing, knowing GDP regulations is a must for you. It prevents a lot of errors and minimizes the chance of being spotted by the regulatory bodies in their audits.
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$199.00
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