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ConferenceDeadline DateCountry
1.The 20th IEEE Symposium on Computers and Communications - Workshops2015-03-302015-07-06Cyprus
2.2015 Special Session on Cognitive-based Text Understanding and Web Wisdom (CTUW2015)2015-03-305013-07-06China
3.2015 International Conference on Artificial Intelligence and Software Engineering2015-05-312015-06-18China
4.10th Pipeline Technology Conference (ptc)2015-01-152015-06-08Germany
5.2015 6th International Conference on Chemical Engineering and Applications2015-06-102015-08-27China
6.2015 2nd International Conference on Biomedical and Bioinformatics Engineering2015-06-102015-08-27China
7.2015 2nd International Conference on Substantial Environmental Engineering2015-06-102015-08-27China
8.Human Factors Engineering2015-03-312015-03-31U.S.A
9.Generation of Controlled Documents and Related Training2015-03-302015-03-30U.S.A
10.Fit for Promoting2015-03-252015-03-26U.S.A
11.Implementing Best Practices for Global Regulatory Intelligence Programs: Dos and Don'ts2015-03-252015-03-25U.S.A
12.U.S. Export Documentation and Procedures2015-03-242015-03-24U.S.A
13.Process Capability Indices for Medical Device Manufacturers2015-03-232015-03-23U.S.A
14.Texting and E-mail with Patients — Meeting Patient Desires Within the HIPAA Rules2015-03-182015-03-18U.S.A
15.China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)2015-03-182015-03-18U.S.A
16.Process Validation - overview of Why and How2015-03-172015-03-17U.S.A
17.GMP Compliance Audit: How Best to Prepare for it2015-03-122015-03-12U.S.A
18.Process Validation Challenges Due to Limited Data and Statistical Comprehension2015-03-112015-03-11U.S.A
19.2015 International Conference on Pharmacology and Toxicology (ICPT 2015)2015-04-292015-06-12China
20.2015 Conference on Pharmacovigilance and Drug Safety (CPDS 2015)2015-04-292015-06-12China
21.Interdisciplinary Chart Analysis-Internal Audits2015-03-232015-03-24U.S.A
22.Guide to Workplace Fire Safety Tips- OSHA Regulations2015-03-302015-03-31U.S.A
23.Live event Human Factors Engineering2015-03-302015-03-31U.S.A
24.Live event What Firms Should Do to Best Prepare for and Manage Audits by EU Notified Body and FDA2015-03-302015-03-31U.S.A
25.Live event Generation of Controlled Documents and Related Training2015-03-292015-03-30U.S.A
26.Live event Implementing Best Practices for Global Regulatory Intelligence Programs:Dos and Don'ts2015-03-242015-03-25U.S.A
27.Live event U.S. Export Documentation and Procedures2015-03-232015-03-24U.S.A
28.Live event Process Capability Indices for Medical Device Manufacturers2015-03-222015-03-23U.S.A
29.Live event Texting and E-mail with Patients—Meeting Patient Desires Within the HIPAA Rules2015-03-172015-03-18U.S.A
30.Live event China:Compliance Processes for Life Science Products (Company Establishment,Clinical Trials,Registrations,Renewals and Supply Chain Considerations)2015-03-172015-03-18U.S.A
31.Live event Process Validation-overview of Why and How2015-03-162015-03-17U.S.A
32.Live event GMP Compliance Audit:How Best to Prepare for it2015-03-112015-03-12U.S.A
33.Live event Process Validation Challenges Due to Limited Data and Statistical Comprehension2015-03-102015-03-11U.S.A
34.Webinar Medical Device Changes and the 510(k)2015-03-312015-03-31Canada
35.Webinar On If It Wasn’t Documented It Didn’t Happen: Legal & Effective Discipline & Documentation2015-03-252015-03-25Canada
36.Webinar On Clean Room Design and Operation2015-03-252015-03-25Canada
37.Webinar On Managing the FDA form "483": Inspection Observations2015-03-242015-03-24Canada
38.Webinar On Metrology: Statistical Analysis of Measurement Uncertainty2015-03-122015-03-12Canada
39.Webinar On Hazard Analysis and Product Risk Management under ISO 14971 and ICH Q92015-03-112015-03-11Canada
40.Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research2015-03-052015-03-05U.S.A
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