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Conference
Deadline
Date
Country
1.
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
2020-07-31
2020-08-10
U.S.A
2.
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
2020-07-06
2020-07-16
U.S.A
3.
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
2020-06-27
2020-07-06
U.S.A
4.
FDA Recalls - Before You Start, and After You Finish
2020-06-15
2020-06-25
U.S.A
5.
The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities
2020-06-12
2020-06-22
U.S.A
6.
Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
2020-06-08
2020-06-18
U.S.A
7.
REACH and RoHS Compliance: Gain a Deeper Understanding
2020-06-01
2020-06-11
U.S.A
8.
How to Conduct an ACH Risk Assessment and Develop an Effective ACH Risk Management Program
2020-06-01
2020-06-11
U.S.A
9.
Work Up and Product Isolation, Virtual Training
2020-06-08
2020-06-09
U.S.A
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