Vendor Selection & Management -By AtoZ Compliance

Thursday, Oct 20, 2016 at 1:00 PM to 2:30 PM EST

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Thursday, Oct 20, 2016 at 1:00 PM to 2:30 PM EST

Key Take Away:

 

This webinar will provide step-by-step considerations for finding potential vendors, implementing a robust qualification & selection process, strategies for oversight and management of vendors, and a risk mitigation approach for key vendors.

 

Overview:

 

GxPs are required to be followed, not only by the sponsoring company, but also by all vendors who are chosen by the company to complete activities that must follow GxPs. These vendors include, but are not limited to, contract research organizations, clinical investigators, manufacturers of drug substance and drug product used in clinical studies and commercialized, labelers and distributors, testing laboratories, warehouses, and so on.

 

Why Should You Attend:

 

In order to ensure selection of vendors who are appropriate to complete the job, companies must have in place a robust program for qualifying vendors, contracting with them, managing and overseeing their activities, and a program for mitigating against risks that may arise related to key vendors.

 

This webinar will address approaches to selecting vendors to perform manufacturing and testing activities as well as clinical study activities. The information obtained will enable implementation of an effective vendor selection program and a comprehensive vendor management and oversight program. The webinar will address aspects of requesting bids, performing audits, evaluating risks, and preparing plans and agreements for effective oversight and management.

 

Areas Covered In This Webinar:

 

•  Making a request for proposal to vendors

 

•  Performing evaluations of vendors

 

•  Auditing potential vendors

 

•  Evaluating business continuity of vendors for long-term relationships

 

•  Establishing comprehensive quality agreements

 

•  Strategy for development of communication plans and oversight activity reviews

 

•  Documenting and monitoring vendor activities

 

•  Value of evaluating back-up vendors

 

 

Learning Objectives:

 

•  Step-by-step considerations for finding potential vendors

 

•  Implementing a robust qualification & selection process

 

•  Strategies for oversight and management of vendors

 

•  Risk mitigation approach for key vendors 

 

 

Who Will Benefit:

 

•  Quality Assurance Personnel

 

•  Quality Control Personnel

 

•  Manufacturing Operations Staff 

 

•  Validation Personnel

 

•  Clinical Operations Staff

 

•  Project Management Team

 

•  Regulatory Affairs Personnel

 

•  Non-clinical Study Personnel

 

For more information, please visit : https://www.atozcompliance.com/trainings-webinar/life-sciences/pharmaceuticals/vendor-selection-management/peggy-j-berry/300152

Email: support@atozcompliance.com 

Toll Free: +1- 844-414-1400

Tel: +1-516-900-5509

 

Level: 

Intermediate

 

Speakers Profile:

Peggy J. Berry

Peggy J. Berry, MBA, RAC, is the President & CEO at Synergy Consulting where she provides consulting services to companies in all aspects of drug development.  She also provides group and one-on-one training in drug development, regulatory affairs and project management topics.  Prior to founding Synergy Consulting in 2015, she was Vice President of Regulatory Affairs at Insmed (2/2015-5/2015) where she was responsible for the development and implementation of global regulatory strategies and the management and oversight of the regulatory affairs department. Prior to Insmed, she was Vice President of Regulatory Affairs and Quality at Amarin (3/2009-2/2014).  

 

She has also held a variety of senior level positions at Dyax (5/2006-3/2009), MGI Pharma (now Eisai; 7/2005-5/2006), AstraZeneca (10/2001-7/2005), and Dey Pharma (now Mylan; 12/1997-10/2001). She has also held Regulatory Affairs roles within two clinical contract research organizations (ILEX Oncology and Cato Research Ltd; 1992-1997) and has worked in review divisions at the FDA (1985-1992).  In addition, Ms. Berry consults for a number of companies in the regulatory and quality area, conducts a number of training courses, and is active in the Regulatory Affairs Professionals Society.  She is the editor of the 2010 book “Choosing the Right Regulatory Career” (RAPS, MD) and author of the 2011 book “Communication & Negotiation” (RAPS, MD).

AtoZ Compliance; is an online compliance webinar training organization based in New Hyde Park, New York. We provide diverse range of quality webinar training programs to all the major segments of industries. Our compliance webinar training programs are designed to meet the changing compliance requirements and we have been successful in conducting high quality training programs to professionals from Fortune 500 to large and medium organizations. We cater to all major industries where FDA regulations and compliance adherence has been extremely critical in the business decision making process. Our compliance webinar training programs focuses on industries such as Life Sciences, Food and Chemicals,Human Resources, Banking and Financial Services,Healthcare and varied other Cross Industry streams. We take extreme care in selecting the topics which are highly relevant to all the industries and are capable of meeting the demands of the complex compliance environment. Our great pool of experienced speakers ensures that your business is up to date with the most relevant and accurate compliance information. At AtoZ Compliance, we focus on our core values - quality, expertise, and customer experience which are the foundation of our business. We believe that our compliance webinar training programs based on our value system can help you grow and succeed in your business.

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