Book Online Tickets for Auditing API Facilities: A MUST to prope, Palo Alto.  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 eit

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

 

  • One Dial-in One Attendee

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    USD 229
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  • Group-Max 10 Attendees or Location

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  • 1x Person - Unlimited viewing for 6 Months

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    USD 299
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  • One CD or USB is for usage in one location only

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    USD 399
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  • LIVE + RECORDED VERSION

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    USD 399
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  • LIVE + TRAINING CD or USB

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    USD 499
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About The Event

 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.