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2 Day Online Analytical Method Validation, Verification and Transfer Course (February 9-10, 2023)
Dublin, Dec. 30, 2022 (GLOBE NEWSWIRE) -- The "Analytical Method Validation, Verification and Transfer [New Course]" training has been added to ResearchAndMarkets.com's offering.
Dependable analytical results are essential to making a knowledgeable choice about the excellence and care of the products in the medicinal business. Additionally, such investigative data is required for supervisory submissions in the provision of the drug creation recordings. Therefore, expressive untried projects including scheme appropriateness limits must be planned for the intended use of the process.
In this course, a general guideline for the determination of the analytical characteristics for different types of validation procedures is highlighted for the analysis of both the drug substance and drug product. The factors to consider for verification of the compendial procedures will also be discussed.
In addition, different approaches for the transfer of analytical procedures from one lab (transferring) to another lab (s) (receiving) under different circumstances will be covered. Other related topics for obtaining reliable data will also be discussed. These topics include analytical instrument qualification as well as how to set, handle and monitor specifications.
In this Analytical Method Validation Training Course, the overall recommendation for the purpose of the logical features for diverse types of authentication measures is highlighted for the examination of the drug substance and drug product.
The trainees will be required to pay attention to the influences to reflect for confirmation of the compendial actions that are an indivisible part of the training course.
In addition, different methods for the transmission of the analytical procedures from one lab (transferring) to another lab (s) (receiving) under different conditions will be enclosed. Other related topics for obtaining reliable data will also be discussed. These themes comprise logical tool requirements as well as how to set, grip and screen specifications.
Learning Objectives
The Analytical Method Validation Training Course follows a few objectives that every aspiring candidate needs to focus on while undergoing the course:
Drug Endorsement Process and Controlling Necessities (secluded values)
Substitute Official methods and options
Allowed Alterations of Chromatographic System Strictures
Pharmacopeias and Compendial Approval Process (public standards)
Logical Method Life Cycle
Investigative Method Authentication
Compendial Coordination Procedure
Analytical Instrument Qualifications including DQ, IQ, OQ, PQ
Analytical Method Verification
Analytical Method Transfer
Chromatography System Appropriateness Necessities
Analytical Method Validation
How to Set Specifications and how to handle out-of-specification (OOS) and out-of-trend (OOT) results
Who Should Attend:
Quality Analysis Managers and Personnel
Controlling Personnel
Analytical and or Formulation Chemists
Quality Control Managers and Personnel
Lab Supervisors and Managers
Compendial Liaisons
Senior or Graduate students (chemistry, pharmaceutical, pharmacy)
Pharmaceutical scientists/Pharmacists working in Industry
Key Topics Covered:
DAY 01 (10:00 AM - 4:00 PM EST)
Seminar objectives review, expectations, and scope.
Pharmacopoeias and Compendial (USP) Approval Process (public standards)
Analytical Method Validation (typical validation parameters)
Drug Approval Process and Regulatory (FDA) Requirements (private standards)
Chromatography System Suitability Requirements
Compendial Harmonization Process
Qualification Phases (DQ, IQ, OQ, PQ)
Precision/Accuracy
Allowed Adjustments of Chromatographic System Parameters
Specificity
Factors to Consider
LOD and LOQ
Analytical Method Verification
Analytical Instrument Qualifications
Analytical Method Transfer
Linearity/Range
FDA and USP Requirements
Instrument Categories
Different Approaches
Summary and Review
DAY 02 (10:00 AM - 01:00 PM EST)
Investigative Procedure Life Cycle
Setting Stipulations FDA rules and ICH strategies (Q6A)
Out-of-Specification (OOS)
Out of Trend (OOT)
How to handle OOS and OOT?
Summary and Review
For more information about this training visit https://www.researchandmarkets.com/r/f65888
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