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Conference
Deadline
Date
Country
1.
Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines
2021-03-01
2021-03-11
U.S.A
2.
Designing and Sustaining New and Existing Product Stability Testing Program
2021-02-22
2021-03-03
U.S.A
3.
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
2021-02-15
2021-02-25
U.S.A
4.
The Veterinary Drug Approval Process and FDA Regulatory Oversight
2021-02-14
2021-02-24
U.S.A
5.
REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance
2021-02-08
2021-02-18
U.S.A
6.
Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)
2021-02-06
2021-02-16
U.S.A
7.
Project Management for Human Resources
2021-01-31
2021-02-10
U.S.A
8.
FDA's Medical Device Software Regulation Strategy
2021-01-30
2021-02-09
U.S.A
9.
Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
2021-01-24
2021-02-03
U.S.A
10.
Social Media Strategies Summit - First Responders | Virtual Conference
2021-02-01
2021-02-02
U.S.A
11.
Change Control Best Practices - Avoiding Unintended Consequences of Changes
2021-01-18
2021-01-28
U.S.A
12.
Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR
2021-01-17
2021-01-27
U.S.A
13.
21 CFR Part 11 Compliance for SaaS/Cloud Applications
2021-01-17
2021-01-27
U.S.A
14.
Data Integrity: FDA/EU Requirements and Implementation
2021-01-11
2021-01-21
U.S.A
15.
REACH and RoHS Compliance: Gain a Deeper Understanding
2021-01-11
2021-01-21
U.S.A
16.
Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
2021-01-11
2021-01-21
U.S.A
17.
Biostatistics for the Non-Statistician
2021-01-10
2021-01-20
U.S.A
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