The presentation will cover the following topics:
> cGMP requirements for cleanrooms.
> Integrated approach towards achieving Validation
- development of Master Plan, BOD, IQ/OQ/PQ
strategies - at the design stage.
- Coordination required of Design Engineering
and Validation groups
- Cost savings due to designing for Validation
- i.e. the Integrated Approach
> End User Role in developing
specifications and resultant cost impacts.
> Basics of Cleanroom Airflow design and
Its impact on OPERATING & INITIAL
COSTS.
- cost and performance advantages of new
modeling techniques
> Comparison of Energy Savings -
Optimized By-Pass Air Handling System
Vs Conventional Air Handling
- Conventional vs. Optimized Bypass
Airhandlers
- Cost comparisons for an ISO 5 Biotech (Tissue Processing) facility
- Cost comparisons for an ISO 7 Biotech Tissue Processing) facility
> Particle Characterization of Process Equipment for suitability of use in Cleanrooms
- This can eliminate many problems in operation and PQ.
Please email "office@technovation.org" and request a registration form. The registration form will indicate the various forms of payment we accept as well as details about the webinar. Once you email your registration form back to us, we will send a confirmation to you via email indicating receipt of your registration. As the date of the webinar draws near, we will email instructions on how to join the webinar, which is approximately two hours long. During our webinar you will be able to commenton the presentation as well as ask questions directly to the presenter.