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Healthcare Training 2020 - Applied Statistics for Scientists and Engineers

Date2020-03-26 - 2020-03-27

Deadline2020-03-26

VenueSFO, CA, USA - United States USA - United States

KeywordsFDA Compliance; Healthcare; Pharmaceutical

Websitehttps://www.globalcompliancepanel.com/se...r_2020_SEO

Topics/Call fo Papers

Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteria and specifications, performing measurement systems analysis (MSA), conducting stability analysis, using design of experiment (DOE) for process development and validation, developing process control charts, and determining process capability indices.
Different statistical methods are required for each of these particular applications. Data and tolerance intervals are common tools used for setting acceptance criteria and specifications. Simple linear regression and analysis-of-covariance (ANCOVA) are used for setting expiries and conducting stability analysis studies. Two-sample hypothesis tests, analysis-of-variance (ANOVA), regression, and ANCOVA are methods used for analyzing designed experiment for process development and validation studies. Descriptive statistics (distribution, summary statistics), run charts, and probability (distributions) are used for developing process control charts and developing process capability indices.
This course provides instruction on how to apply the appropriate statistical approaches: descriptive statistics, data intervals, hypothesis testing, ANOVA, regression, ANCOVA, and model building. Once competence in each of these areas is established, industry-specific applications are presented for the participants.
Why should you attend:
21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries specify the application of statistical methods across the product quality lifecycle.
According to the Quality System Regulation (QSR) for medical devices, "Where appropriate, each manufacturer shall establish and maintain procedures for identifying valid statistical techniques required for establishing, controlling, verifying the acceptability of process capability and product characteristics." Although there are many statistical method that may be applied to satisfy this portion of the QSR, there are some commonly accepted methods that all companies can and should be using to develop acceptance criteria, to ensure accurate and precise measurement systems, to fully characterize manufacturing processes, to monitor and control process results and to select an appropriate number of samples.
According to both 21 CFR and guidance documents, the need for statistical methods is well established from discovery through product discontinuation. 21 CFR specifies the "the application of suitable statistical procedures" to establish both in-process and final specifications. The guidance documents necessitate the application of statistical methods for development and validation of measurement systems, process understanding using Quality by Design (QbD) principles, process validation, as well as ensuring the manufacturing process is in control and is capable.
This course provides instruction statistical methods for data analysis of applications related to the pharmaceutical, biopharmaceutical, and medical device industries.
Areas Covered in the Session:
Objectives:
describe and analyze the distribution of data
develop summary statistics
generate and analyze statistical intervals and hypothesis tests to make data-driven decisions
describe the relationship between and among two or more factors or responses
understand issues related to sampling and calculate appropriate sample sizes
use statistical intervals to setting specifications/develop acceptance criteria
use Measurement Systems Analysis (MSA) to estimate variance associated with: repeatability, intermediate precision, and reproducibility
ensure your process is in (statistical) control and capable
Who Will Benefit:
This seminar is designed for pharmaceutical, biopharmaceutical, and medical device professionals who are involved with product and/or process design:
Process Scientist/Engineer
Design Engineer
Product Development Engineer
Regulatory/Compliance Professional
Design Controls Engineer
Six Sigma Green Belt
Six Sigma Black Belt
Continuous Improvement Manager
Event link: https://www.globalcompliancepanel.com/seminar/-901...
Contact Info:
Netzealous LLC - Globalcompliancepanel
Phone No: 1-800-447-9407
Fax: 302 288 6884
Email: globalcompliancepanel-AT-gmail.com
Website: https://www.globalcompliancepanel.com/

Last modified: 2019-12-06 22:07:16