Records in Finished Dose Manufacturing
This Module is aimed at personnel who work in the pharmaceutical and biopharmaceutical industries and maintain records for finished dose manufacturing in accordance with GMP Regulations, including records of materials, production records, equipment records, laboratory records, production review and distribution records.
Whether for onboarding or annual refresher training, this Module is seamlessly deployable on any LMS and can be tailored to your company’s exact needs.
Duration: 30 Mins
Description
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Module Features:
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