ComplianceOnline

Implementing Disposable Technologies in a GMP Facility: A case study

Instructor: Peter K Watler
Product ID: 701397
Training Level: Intermediate
  • Duration: 90 Min

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

$500.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

This Disposable Technologies training webinar in GMP Facility will guide you through the practical aspects of implementing disposable technologies and offer superb control of process stream contaminants such as endotoxins and bioburdens.

The 21st century has seen the introduction of increasingly diverse and competitive single-use technologies for Bioprocessing. This case study will highlight the extensive implementation of disposable filters, vessels, connectors, mixers, sampling devices and bulk storage containers in a GMP facility. The use of disposable technologies enabled facility design and construction in only 12 months at a modest cost of only $13 million.

A hybrid approach to facility design was employed to leverage the benefits of conventional equipment by augmentation with new disposable technologies. Disposable technologies benefited the project through reduced capital outlay, shorter equipment lead times, faster construction and rapid startup, enabling aggressive cost and timeline targets to be met. Disposable technologies enhanced GMP operation by offering superb control of process stream contaminants such as endotoxins and bioburdens.

Implementing such leading-edge technologies brings new challenges, especially for change control, vendor selection and validation. This discussion will also focus on practical aspects of implementing disposable technologies, including:

  • Accelerated Timeline Management.
  • Supply Chain Management (preferred vendor selection, change control).
  • Regulatory Advantages (closed processing, eliminate cross-contamination).
  • Streamlining Operations (tank farm flexibility).
  • Validation savings and challenges (mixing, extractable, leachables).

Areas Covered in the seminar:

  • Highlight extensive implementation of disposables in a Bioprocessing facility.
  • How a hybrid approach was employed for facility design.
  • Challenges that occurred in the implmentation.
  • Cost effectiveness.
  • Process control benefits.
  • Supply chain management and time management changes.
  • How well planned implementation can produce streamlined operations.
  • Validation benefits.

Who will benefit:

  • End-users responsible for applications that need to be validated
  • QA managers and personnel
  • Engineering, commissioning, process design professionals
  • Validation specialists
  • Consultants
  • Quality system auditors

Instructor Profile:
Peter K. Watler, Ph.D is Principal Consultant and Chief Technology Officer with Hyde Engineering + Consulting. He has 22 years of GMP biopharmaceutical process experience with a focus on process design, scale-up, implementation and facility design, start-up and qualification. He has prepared 3 license submissions and participated in several FDA inspections and GMP audits.

Dr. Watler was previously Vice President, Manufacturing at VaxGen, where he led the design, construction, commissioning and qualification of a GMP vaccine facility. He was also responsible for managing supply chain and production operations, led the CMC team and prepared submissions for government agencies. He previously spent 12 years at Amgen, leading process development, manufacturing support and overseeing pilot plant operations. He has led teams for technology transfer, scale-up, pre-clinical production and process validation for Neupogen®, Stemgen®, Kepivance® and Infergen®. Dr Walter holds a Bachelor’s and a Master’s degree in Chemical Engineering from the University of Toronto and a Ph.D. in Chemical Engineering from Yamaguchi University, Japan.

Follow us :
ComplianceOnline Medical Device Summit 2017
FDA's New Import Program for 2017 - Strict Precision

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. ComplianceOnline 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.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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