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FDA Regulatory Rules for Supply Chain and Manufacturing from 2017 Through 2022
This Webinar is over| Date | May 19, 2017 |
| Time | 10:00 AM EDT |
| Cost | $299.00 |
|
Online
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Short Abstract
In this webinar, we will discuss all essential regulatory rules for Supply Chain and Manufacturing
Key Areas Covered During the Webinar:
1.Introduction: Counterfeit Crisis and 2001 Initiative
Registration Information
In this webinar, we will discuss all essential regulatory rules for Supply Chain and Manufacturing
Key Areas Covered During the Webinar:
1.Introduction: Counterfeit Crisis and 2001 Initiative
- Industry and FDA Response: Track and Trace
- Drug Supply Chain Security Act (DSCSA)
- Continuous auditing systems, ISO 9000/14000
- 21CFR Part 11, GMP GLP GCP
- Compliance Management.
- Proactive Risk Balance.
- Integrated Risk Management Process.
- Global Standards One (GS-1).
- Open Serialization Communication Standard and Electronic Product Code Information Services (EPCIS).
- in close coordination with the FDA and the EMA in Europe; which in turn as set up the standards found in DSCSA.
- Track and Trace Vendors
- Product tracing across the value chain
- Detection response from all to identification of countefet
Registration Information
- Registration Fee : USD $299
- For assistance on registration, please send an email tomarketing@biopractice.com or Please call: Ph - 1-646-216-8860
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