One day (8 Hr) Training Program on
Good Laboratory Practices (GLP) for Non-clinical Laboratory Studies
Speaker: Dr. M. Imran Khan, Expert Consultant – GLP
Course Description:
This Good Laboratory Practice (GLP) nonclinical training course introduces learners to the general requirements of the Principles of Good Laboratory Practice for the conduct of nonclinical health and environmental safety studies as outlined in the OECD GLP. Complying with OECD Principles of GLP is an imperative step for future drug development /product applications to regulatory authorities, across the globe who review new drug /product applications.
This course on Good Laboratory Practice (GLP) is intended for those who wish to understand and learn the fundamentals of Good Laboratory Practices and the requirements for GLP compliance in non-clinical laboratories.
The course is carefully designed to cover details on the roles and responsibilities of the Test Facility Management and Study Director in planning, supervising, and managing nonclinical studies. The requirements for Test Facility Organization and personnel, Quality Assurance program, Standard Operating Procedures (SOPs), Performance of Study, Reporting of the Study Results, Training of Staff, Good Documentation Practices, The Conduct and Performance of the Study under GLP. The requirements for the conduct of the GLP-compliant laboratory study to assure animal welfare, data integrity, and thorough chain-of-custody of specimens and materials will be discussed.
Why Attend This Program?
After completion of the GLP training course, you will learn about the fundamentals of GLP- Good Laboratory Practices, the requirements for GLP compliance, and record-keeping as per the OECD principles of GLP.
This 8-hour training course will be conducted by our GLP experts who have more than two decades of experience working in GLP-compliant labs and have given GLP consultation services to numerous organizations from diverse industries. The experts will share their experiences and knowledge of best practices being followed for GLP compliance.
Course Outline:
The schedule for a one-day GLP training program is four sessions of 2 hours each. Each session will have 90-100 min of talk or presentation, followed by 20-30 min of discussion / Q&A session.
Session 1:
Introduction to Principles of GLP covering the ten primary elements of GLP.
Session 2:
- Responsibilities of Test Facility Management
- Roles and Responsibilities of Study Director and Study Personnel
Session 3:
- Quality Assurance Unit and GLP, including the responsibilities of QAU
Session 4:
- The Conduct and Performance of the Study under GLP
8-Hour Training Program Agenda:
Session 1: 09:00 am to 11:00 am IST
Tea break: 11:00 to 11:15 am IST
Session 2: 11:15 am to 01:15 pm IST
Lunch break: 01:15 to 02:00 pm IST
Session 3: 02:00 pm to 04:00 pm IST
Tea break: 04:00 to 04:15 pm IST
Session 4: 04:15 pm to 06:00 pm IST
Who Should Attend?
The following individuals or disciplines will benefit from attending this training program:
- Principal Investigators, Study Directors, Study Monitors
- Scientists and Research Staff, Laboratory Managers
- R&D Personnel, Lab technicians, Lab Analysts
- Regulatory and Compliance Managers
- Quality Assurance personnel
- Quality System Auditors
- CRO staff
- CRO Managers (Accredited Laboratories)
This 8-hour training program is ideal for new or experienced staff of the following industries (Non-clinical Testing)
- Pharmaceuticals
- Medical Device
- Food
- Nutraceuticals
- Agrochemical
- Cosmetics
Employee / Corporate Training:
For corporations seeking a method to train employees economically, Zyirn Research Consultancy is the training partner you can rely on. Our training provides an effective, engaging, and in-depth learning experience for all laboratory personnel working in a non-clinical testing environment. We cater to both small-scale and large-scale training requests, with the same goal: To make this a good experience for everyone involved, from the students to those managing the GLP-compliant labs.
Group Discounts:
We offer online and on-site Good Laboratory Practice training and consultation services for organizations with 10 or more employees enrolling. Contact us today at [email protected] or give us a call at +91 -9820310424 / +1 403.604.7869 for course details and group discounts
Please read the below instructions before registering for the webinar
- Register with a valid email id and phone number. Webinar link will be shared with registered participants. Registered participants can log in only from one device at a time.
- Kindly mention your Full Name with prefix (Dr./Mr./Mrs./Ms) while registering (The same details will be used on the Certificate Of Participation)
- Multiple logins using the same ID will not be allowed in the Webinar. (such as the same User ID being used by multiple users).
- “Certificate Of Participation” will be issued to those who attend the sessions.
- “Certificate Of Participation” will be provided in a week from the date of the sessions .
- Registration Fees can be paid via Google Pay or Pay U money
The schedule for a one-day GLP training program is four sessions of 2 hours each. Each session will have 90-100 min of talk or presentation, followed by 20-30 min of discussion / Q&A session.