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    ConferenceDeadline DateCountry
    1.Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines2021-03-012021-03-11U.S.A
    2.Designing and Sustaining New and Existing Product Stability Testing Program2021-02-222021-03-03U.S.A
    3.Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions2021-02-152021-02-25U.S.A
    4.The Veterinary Drug Approval Process and FDA Regulatory Oversight2021-02-142021-02-24U.S.A
    5.REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance2021-02-082021-02-18U.S.A
    6.Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)2021-02-062021-02-16U.S.A
    7.Project Management for Human Resources2021-01-312021-02-10U.S.A
    8.FDA's Medical Device Software Regulation Strategy2021-01-302021-02-09U.S.A
    9.Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers2021-01-242021-02-03U.S.A
    10.Social Media Strategies Summit - First Responders | Virtual Conference2021-02-012021-02-02U.S.A
    11.Change Control Best Practices - Avoiding Unintended Consequences of Changes2021-01-182021-01-28U.S.A
    12.Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR2021-01-172021-01-27U.S.A
    13.21 CFR Part 11 Compliance for SaaS/Cloud Applications2021-01-172021-01-27U.S.A
    14.Data Integrity: FDA/EU Requirements and Implementation2021-01-112021-01-21U.S.A
    15.REACH and RoHS Compliance: Gain a Deeper Understanding2021-01-112021-01-21U.S.A
    16.Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact2021-01-112021-01-21U.S.A
    17.Biostatistics for the Non-Statistician2021-01-102021-01-20U.S.A
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