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1.长期征稿Ei Compendex;Scopus ;ISI Web of Science 检索的会议2080-12-292080-12-30U.S.A
2.长期征稿EI(EI Compendex)ISTP(科学技术会议录索引)会议论文集2080-12-292080-12-30U.S.A
3.长期征稿CPCI检索会议论文 版面费用全国最低 最优惠 长期征稿2080-12-292080-12-30U.S.A
4.2014 National Hepatitis B&C Training Program and Treatment Update2018-06-282027-09-27U.S.A
5.Essentials Of USP Microbiology - Reading Between the Lines of the USP General and Information Microbiology Chapters2020-06-152020-06-25U.S.A
6.17th International RAIS Conference on Social Sciences and Humanities2020-04-052020-06-01U.S.A
7.Biocompatibility Testing for Medical Devices2020-04-272020-05-07U.S.A
8.Current Concepts in Resuscitation2020-04-302020-05-01U.S.A
9.Managing Your FDA Inspection: Before, During and After2020-03-232020-04-02U.S.A
10.Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devices, IVDs)2020-03-232020-04-02U.S.A
11.16th International RAIS Conference on Social Sciences and Humanities2020-02-252020-03-30U.S.A
12.Applied Statistics for Scientists and Engineers2020-03-262020-03-27U.S.A
13.Data Integrity: FDA/EU Requirements and Implementation2020-03-162020-03-26U.S.A
14.FDA Recalls - Before You Start, and After You Finish2020-03-162020-03-26U.S.A
15.Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies2020-03-162020-03-26U.S.A
16.Internal Audit, Fraud Risk Assessment and Risk Management Annual Plan2020-03-162020-03-26U.S.A
17.Clinical Data Management (CDM)2020-03-162020-03-26U.S.A
18.Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)2020-03-132020-03-23U.S.A
19.Biostatistics for the Non-Statistician2020-03-132020-03-23U.S.A
20.Preparing for FDA's New Import/Export Trauma in 20202020-03-092020-03-19U.S.A
21.15th International Conference on Cyber Warfare and Security2019-08-212020-03-12U.S.A
22.Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada2020-02-242020-03-05U.S.A
23.A Comprehensive View of FDA Regulations for Medical Devices2020-02-242020-03-05U.S.A
24.FDA Audit, Quality Assurance Practices, Responsibilities and Expectations2020-02-172020-02-27U.S.A
25.HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer2020-02-162020-02-26U.S.A
26.HIPAA, Consents, and 42 CFR Part 2 - Tracking the Release of Information Under Conflicting Rules2020-02-202020-02-20U.S.A
27.Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)2020-02-102020-02-20U.S.A
28.California Leaves of Absence - Employer Obligations, Leave Interactions, and Handling Problems and Performance Management Challenges - PDL, FMLA, FEHA, SDI, CFRA, PFL, ADA, and Workers Compensation2020-02-102020-02-20U.S.A
29.Designing and Sustaining New and Existing Product Stability Testing Program2020-02-032020-02-13U.S.A
30.FDA's Medical Device Software Regulation Strategy2020-02-032020-02-13U.S.A
31.Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices2020-01-272020-02-06U.S.A
32.Analytical Instrument Qualification and System Validation2020-01-272020-02-06U.S.A
33.REACH and RoHS Compliance: Gain a Deeper Understanding2020-01-272020-02-06U.S.A
34.Why is FDA at my facility, and what do I do during an inspection?2020-01-272020-02-06U.S.A
35.Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines2020-01-242020-02-03U.S.A
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