Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection

Conferences

Health and Medicine

Added by Referral on 2019-04-12

Conference Dates:

Start Date: 2019-05-15
Last Date

Last Day: 2019-05-15

Deadline for abstracts/proposals: 2019-05-13

Conference Contact Info:

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]

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Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection

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Conference Description:

In this FDA inspection webinar attendees will learn the basic understanding of Active Pharmaceutical Ingredient Good Manufacturing Practices (ICH Q7) and the most important elements of API GMP to avoid serious deviations and failures during either a Pre-Approval or GMP Inspection.

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