FDA’s Expectations from Supplier Management for GMP: Quality Agreements and More

Added by Referral on 2019-04-18

Conference Dates:

Start Date Start Date: 2019-06-13
Last Date Last Day: 2019-06-13
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2019-06-11

Conference Contact Info:

Contact Person Contact Person: Ashutos Swain
Email Email: [email protected]
Address Address: 2479 E. Bayshore Road Suite 260, Palo Alto, CA, 94303, United States
Phone Tel: 8887172436
Phone Fax: [email protected]

Conference Description:

The FDA requires that manufacturers of pharmaceutical products have a documented process to assess its suppliers and contract manufacturers, that they have implemented that process, and that the process is effective. This training program will explore how having an effective supplier relationship management program will result in streamlining the supply chain, ensuring a more consistent level of quality components, materials and components, and be more cost effective to the manufacturer.
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