Selection and Use of (Certified) Reference Material in Analytical Laboratories

This training on using certified reference material in analytical laboratories will cover FDA and international requirements for selection, purchasing, testing, storage and use of (certified) reference material.

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One User Unlimited access to all recorded webinars for 6 Months

Recorded Version Only

(PPT + Recorded Streaming Link)

1x Person - Unlimited viewing for 6 Months (For multiple locations contact Customer Care)
rec Recorded Link and Ref. material will be available in My Account Section
Last Recorded Date: Mar-2019

Download File Only

(PPT + Recorded Training File)

Downloadable file is for usage in one location only.
(For multiple locations contact Customer Care)
Downloadable link along with the materials will be emailed within 2 business days
Customer Care

Fax: +1-650-362-2367


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Free Hand-Outs:For easy implementation, attendees will receive
  • 4 SOPs
    • Handling (Certified) Reference Material
    • Purchasing and Receipt of Supplies for Laboratories
    • Quality Assessment of Laboratory Suppliers
    • Preparation of Laboratory Working Standards
  • Checklist: Handling (Certified) Reference Material
Learning Objectives:
  • The role and importance of reference material in chemical measurement
  • FDA and international requirements
  • Requirements of ISO 17025 and ISO 34
  • Official and industry guidance documents
  • Hierarchy of reference material
  • Preparation and Testing of Certified Reference Material
  • Traceability of primary/secondary standards and reference material
  • Preparing working standards from primary and secondary standards
  • Developing an SOP for preparation of working standards
  • Assessment of suppliers of reference materials
  • Practical approaches for qualification of incoming material
  • Optimizing the uses and the costs of reference materials
  • Documentation for the FDA and ISO
Who Will Benefit:

Pharmaceutical development companies, API manufacturers and contract laboratories will benefit from this training. Personnel who will benefit include

  • Analysts
  • Lab Supervisors and Managers
  • QA managers and personnel
  • Consultants
Instructor Profile:
Dr. Ludwig Huber Dr. Ludwig Huber

Director and Chief Editor, Labcompliance

Dr. Ludwig Huber, Ph.D., is the director of Labcompliance and editor of, the global online resource for validation and compliance. He is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems". He has given multiple presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world. This included seminars, workshops and presentations for the US FDA, China SFDA, Korea MFDS, Singapore HSA, ISPE, Japan PDA, PIC/S and several other national health care agencies.

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. FDATrainingAlert would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

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