Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach Course (April 24-26, 2023)
DUBLIN, March 16, 2023 /PRNewswire/ -- The "Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach Course" training has been added to ResearchAndMarkets.com's offering.
Supplier or vendor qualification is a crucial component in compliance to 21 CFR 111. The FDA requires that manufacturers of dietary supplements must "qualify" each of their vendors but do not provide guidance on how a company is to perform this qualification. Supplier qualification principles also apply to subcontracted services affecting cGMP (manufacturing steps, packaging and labeling, testing and/or calibration services, storage and distribution, etc.) Any supplier qualification program must include two critical components:
- Clearly defined specifications/requirements for all of these goods or services being purchased, and;
- Objective evidence to show that your requirements are being consistently fulfilled.
This eight-hour vendor qualification audit training will help you improve the quality in your facility. It is designed for those who already have a basic understanding of dietary supplement GMPs and the knowledge and skills necessary to qualify suppliers.
Since the evaluation of all types of suppliers often involves auditing, this course will incorporate a fresh look at the auditing process and the skills and techniques needed to get the most from these activities. The skills and techniques learned are independent of the type of auditing or the standard being audited and will be useful when conducting internal audits and performing audits of suppliers.
Why Should You Attend
The various regulatory agencies have expectations that suppliers and vendors will demonstrate control over their manufacturing processes, validations, and documentation. Quality auditing is the process of checking whether these organizations have implemented what they have stated in written procedures and whether their people are doing what the organizations procedures state they will do.
On conclusion of this course, you will have an understanding of the following:
- Regulations that apply to vendor qualification (21 CFR 111)
- Food Safety Modernization Act (FSMA)
- Impact of FSMA on supplier qualification
- Risk assessment and risk management
- Supplier monitoring activities
- On-site audit strategies and requirements
- Managing the audit process effectively before, during and after
- The consequences of noncompliance
Who Should Attend:
This intensive, practical course will be of value to those professionals in the pharmaceutical, medical device and related industries who are responsible for or involved in any interaction with suppliers, including those working in:
- Regulatory Affairs
- Documentation Management
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.
Utilizing strategic thinking, risk based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.
For more information about this training visit https://www.researchandmarkets.com/r/5hssyj
ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.
Research and Markets
Laura Wood, Senior Manager
For E.S.T Office Hours Call +1-917-300-0470
For U.S./CAN Toll Free Call +1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
View original content:https://www.prnewswire.com/news-releases/auditing-and-qualifying-suppliers-and-vendors---an-effective-risk-based-approach-course-april-24-26-2023-301774463.html
SOURCE Research and Markets
Upcoming Life Sciences Events
- March 2023
- Zurich: Swiss Nordic Bio 2023
- April 2023
- Basel: Swiss Biotech Day 2023
- London: BioTrinity 2023
Latest company news
Vaccitech Reports Full-Year 2022 Financial Results and an Update on Corporate Developments
OKYO Pharma Announces PDMR Dealing
Global Lung Cancer Diagnostics Strategic Analysis Report 2023: Market to Reach $4.7 Billion by 2030 - Increasing Prevalence and Incidence of Lung Cancer to Push the Demand for Early Diagnoses