GMP Training for Manufacturing and Administration Personnel

If you read the FDA quality system regulation clause 820. 25 (personnel) it states that: "Each manufacturer shall establish procedures for identifying training needs and ensure that all personnel are trained to adequately perform their assigned responsibi
Training shall be documented". The term "all personnel" is a very important part of this clause. Very often we provide GMP training to those individuals who work within the disciplines of engineering, regulatory and quality. Furthermore we usually depend on the quality assurance personnel or those regulatory personnel within our organization to be the key providers of information during an FDA QSIT investigation. There may be times when the FDA will want to speak with all disciplines within an organization from the CEO on down. All personnel means "all personnel", which means that anyone involved in the design, manufacture, inspection, test, packaging, and/or service of the device should have adequate training to the GMP requirements.
For More Information Contact -
Organization: NetZealous BDA GlobalCompliancePanel
Website: www.globalcompliancepanel.com/
Email: [e-mail]
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[@irinasegovia4900]

Can we find the slides for free download anywhere? Thanks

[@flosrhythm]

you can find this on google in pdf form.

[@deeppatidar8103]

@@flosrhythm
Plz Can you share links for pdf