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ConferenceDeadline DateCountry
1.Tools for Human Error Reduction2020-02-252020-02-25U.S.A
2.Trump’s Tariffs: Sections 201, 232, and 301: What You Need to Know2020-02-182020-02-18U.S.A
3.Strategic Interviewing & Selection: Getting the Right Talent on Your Team2020-02-142020-02-14U.S.A
4.Emotional Intelligence in Leadership2020-02-142020-02-14U.S.A
5.Excel Tools of the Trade: Every Day Excel Hacks You Need To Know2020-02-142020-02-14U.S.A
6.Handling the Difficult Employee2020-02-132020-02-13U.S.A
7.Importing and Exporting by U.S. Mail and Express Consignment2020-02-132020-02-13U.S.A
8.Leadership: Strategic Planning and Decision Making2020-02-122020-02-12U.S.A
9.Leadership in Adversity2020-02-122020-02-12U.S.A
10.Medical Marijuana in the Workplace2020-02-122020-02-12U.S.A
11.Leadership: Strategic Planning and Decision Making2020-02-122020-02-12U.S.A
12.Tools & Strategies on How to Prevent Making Mistakes2020-02-122020-02-12U.S.A
13.Writing Payroll Procedures2020-02-112020-02-11U.S.A
14.Excel Spreadsheet Validation-Step-by-step guide to data integrity compliance2020-02-112020-02-11U.S.A
15.Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations2020-02-062020-02-06U.S.A
16.GDPR Compliance2020-02-042020-02-04U.S.A
17.3000018 An Advanced Course on Lean Documents, Lean Configuration, and Document Control2020-02-042020-02-04U.S.A
18.Post-Market Activities in the EU-MDR — A Detailed Analysis2020-01-302020-01-30U.S.A
19.Supervising a Human Error Free Environment: You can do a Lot More than you Think2020-01-302020-01-30U.S.A
20.Are you aware FDA’s New Import Program : Be Prepared and Be Compliant2020-01-292020-01-29U.S.A
21.FDA Regulations for Analytical Instrument Qualification and Validation Processes2020-01-282020-01-28U.S.A
22.How to prepare a standard operating procedure (SOP)2020-01-282020-01-28U.S.A
23.Artificial Intelligence (AI) in the Food Supply Chain2020-01-272020-01-27U.S.A
24.Annual Product Quality Reviews; Preparation & Reports - FDA, EU, & Canada Regulatory Requirements2020-01-242020-01-24U.S.A
25.Good Documentation Practice (GDocP) for FDA Regulated Industries2020-01-232020-01-23U.S.A
26.Project Management for Non-Project Managers in the Life Sciences2020-01-232020-01-23U.S.A
27.Understanding Aseptic Technique and Cleanroom Behavior2020-01-212020-01-21U.S.A
28.Excipients: Compliance with Compendial and GMP Requirements2020-01-212020-01-21U.S.A
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