Qualify Your Vendors – Designing and Implementing a cGMP-Compliant Vendor Program| Oct. 24, 2013, 2 PM EDT | Graham

Qualify Your Vendors – Designing and Implementing a cGMP-Compliant Vendor Program| Oct. 24, 2013, 2 PM EDT | Graham

August 21st, 2013 // 8:10 pm @

This new Webinar will provide you with exact details of what you need to do to design a fully cGMP compliant vendor program for your pharmaceutical or medical device supply chain. You will learn how to implement it throughout your company, how to deal with all documentation issues, and how to communicate efficiently with your vendors about your company’s issues and requirements.

Topics Covered

This Webinar will assist you in developing and implementing the most effective, cGMP-compliant vendor program. The following critical information will be delivered:

  1. What you need from vendors and how to evaluate each one
  2. What your employees need to know
  3. How to learn vendor capabilities
  4. How to manage your vendors, based upon their abilities
  5. How to create strong communication between your company’s stakeholders and your vendors
  6. How to manage a vendor program based on your needs

Who Should Attend

This vendor qualification webinar is relevant personnel/ companies in the biotechnology and pharmaceutical industry. The employees who will benefit most include:

  • Senior management
  • Quality Assurance
  • Research and Development
  • Supply chain personnel
  • Project management
  • Process scientist
  • Regulatory Affairs
  • Audit

With your order, we would like to offer you these six items at no added cost:

  • Powerpoint slides to share
  • Downloadable recording
  • Article – 21 CFR Part 11 Enforcement – Where Is FDA Headed? By John Avellanet, Cerulean Associates
  • Article – 10 Ways to Control Compliance Costs – By John  Avellanet, Cerulean Associates
  • Guide – An Executive Guide to Quality by Design – By John Avellanet, Cerulean Associates
  • Newsletter – FDA Digest – By Expertbriefings.com. Latest FDA regulatory news, and recent 483 and warning letter analysis – 12 issues only $399.00

Background

It is impossible for any single company to provide all of the possible needs for cGMP and GLP compliant supplies. There is a major need to be able to adjust on suppliers due to changes in needs, supplier issues, budgets and many other issues.

To be able to manage your pharmaceutical/device vendors, you will need to know what materials you need, how to get them delivered, what information is needed for regulatory needs and how you should properly manage your relationships with vendors, as needs change. You will learn in this 90 minute Webinar how you can effectively develop, maintain and implement these essential relationships with your vendors.

Also, you will grasp how to better communicate with your internal stakeholders about these vital relationships, so you can better communicate the needs of your organization. Remember that no good vendor program works right without total buy in from everyone in your company. We will help to reveal some of the key issues in managing vendor needs.

After this 90 minute Webinar, you will have a good understanding of how to create and manage a highly agile, efficient and compliant vendor program that is cost effective and meets all of your needs. You also will be able to deal with vendors in a clear manner, which will ensure they provide you with all of the materials you require to make your drug and device products.

About the Speaker

Todd Graham is a medical technologist and a bench scientist of the master’s level, with a high degree of expertise in both the clinical diagnostics and biotechnology fields. He has work for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. He has a broad level of expertise in assay development for quality control, pharmaceutical development and clinical diagnostics. His particular levels of expertise are molecular diagnostics, PCR, ELISA, quality control and training of bench level personnel in clinical diagnostics and biotechnology. He is also in the process of establishing a consultancy that assists academic labs in transitioning their research to industry by verifying and improving the quality of their work.

Price: One Webinar Seat $159 (Contact Us for Multiple Webinar Seats)


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