4-Hour Virtual Seminar on Good Laboratory Practices (GLPs) Comparing and Contrasting GMP
The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
Speaker: Joy McElroy | View Anytime | Duration: 4 Hours | Price: ¤495.00 | View Details
6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices)
This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated with the perspectives of Instrument Control, System Suitability Test (SST), Analytical Methods Validation and ensuring Data Integrity for Regulatory Compliance.
Speaker: Joy McElroy | View Anytime | Duration: 6 Hours | Price: ¤595.00 | View Details
GLPs: How are they Associated with GMPs and SOPs
Good Laboratory Practices (GLPs), CFR part 58 is a set of guidelines for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA.
Speaker: Joy McElroy | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Writing Validation Master Plans; Best Practices for Writing a Compliant Document
This webinar will discuss the major components of Validation Master Plans. It will discuss how the VMP is different from Validation SOPs.
Speaker: Joy McElroy | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
GLPs: How are they Associated with GMPs and SOPs
In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details
GLPs: How are they Associated with GMPs and SOPs
In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details
GLPs: How are they Associated with GMPs and SOPs
In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details
GLPs: How are they Associated with GMPs and SOPs
In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details
GLPs: How are they Associated with GMPs and SOPs
In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details
FDA Regulations for Environmental Monitoring(EM) Program
Upon completion of this training, you will be able to Describe how Clean room Environmental Monitoring (EM) Program fits into the Regulations. Explain the basis of the Four (4) Phases of Clean room transitional monitoring (Pre-qualification through post-qualification EM) and what each type stands for. List the basic content of a well-designed, effective and compliant EM Program. Explain the relationship between an EM Excursion Program and CAPA
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details
Best Practices for an Effective Cleaning Validation Procedures
In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system.
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details
FDA Regulations for Analytical Instrument Qualification and Validation Processes
In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system.
Speaker: Joy McElroy | View Anytime | Price: ¤190.00 | View Details