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Konferenzen zum Thema Pharmakologie und Arzneimittelentwicklung in China
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| 3.3rd Annual Clinical Trial Supply China | | Termin | 28. Feb 2012 → 29. Feb 2012 | [ID=444821]  | | Ort | Peking, China | | Zusammenfassung | Key Word/Main Key Words
Pharmaceutical, biopharmaceutical, clinical trials, clinical supply, clinical operation, clinical logistic, licensing, cold chain, supply chain, logistics, transportation, distribution, temperature maintenance/monitoring, quality assurance, IVRS, Good Clinical Practice (GCP), clinical Good Manufacturing Practice(cGMP), Good Distribution Practice (GDP), Good Storage Practice (GSP), warehouse management, risk management, cost saving, Track & Trace Technology, storage, Contingency Plan, regulatory compliance, Third-Party Logistics (3PL), software applications, Temperature-Sensitive-Products (TSPs), Contract manufacturing organisation (CMO), Supply chain management (SCM), Interactive Voice Response System (IVRS), bar-code, clinical trial blind code, labeling
Topic Key Words:
Clinical trials, clinical supply, supply chain, distribution, logistics, cold chain, quality assurance, reduce cost, packaging, labeling, IVRS, Good Clinical Practice (GCP), Good Distribution Practice (GDP)
3rd Annual Clinical Trial Supply China
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The ONLY EVENT Focused on Clinical Trial Supply Chain Management in China
3rd Annual Clinical Trial Supply China 2012 is the only gathering of its kind globally and has been developed through extensive research with over 100 clinical trials supply chain professionals involved with the China market. 3rd Annual Clinical Trial Supply China 2012 will address the most urgent concerns and challenges faced by these professionals in the importation, forecasting, storage and distribution of temperature sensitive clinical trials supplies and samples.
What?s New in 2012?
? Presents two annual events - 3rd Annual Clinical Trial Supply China and 2nd Annual Bio/Pharma Cold Chain China that features content and case-studies that address the unique supply chain needs in China pharmaceutical industry.
? Regulatory updates from Chinese regulators including SFDA, Ministry of Health, Custom, Ministry of Science and Technology on distribution of temperature controlled product and clinical trials supply materials
? International regulatory perspective from US FDA and MHRA on new global updates
? Meet and network with more than 200+ key stakeholders in the China bio/pharma supply chain industry
? 15 rountable discussions topics participate to overcome your day to day supply chain challenges
? FIRST and ONLY supply chain Award for pharmaceutical industry in China
Reasons to Exhibit at 2nd 3rd Annul Clinical Trial Supply China 2012
1. Exhibiting in front of a highly qualified audience will generate leads and accelerate your sales cycle
2. Your presence and visibility builds loyalty with your clients to consolidate your market position
3. Positioning yourself a step forward from other vendors for competitive advantage
4. You will reinforce that your company is an essential partner to the pharmaceutical supply chain industry
5. Demonstrate your strength as well as taking this as an opportunity to display a new product or service
6. Maximise your sales team?s time by providing direct face-to-face access to the industry?s decision makers
7. Showcase your solutions and run product demos to drive demand
8. Our team will work with you to ensure that you meet the people who are important to you
For further details:
1. Visit us at http://www.clinicaltrialssupply.com/Event.aspx?id=628228&MAC=DL
2. Email us at enquiry@iqpc.com.sg with your full contact details
3. Call us at +65 6722 9388 | | Themen | Pharmaceutical, biopharmaceutical, clinical trials, clinical supply, clinical operation, clinical logistic, licensing, cold chain, supply chain, logistics, transportation, distribution, temperature maintenance/monitoring, quality assurance, IVRS, Good Clinical Practice (GCP), clinical Good Manufacturing Practice(cGMP), Good Distribution Practice (GDP), Good Storage Practice (GSP), warehouse management, risk management, cost saving, Track & Trace Technology, storage, Contingency Plan, regulatory compliance, Third-Party Logistics (3PL), software applications, Temperature-Sensitive-Products (TSPs), Contract manufacturing organisation (CMO), Supply chain management (SCM), Interactive Voice Response System (IVRS), bar-code, clinical trial blind code, labeling | | Webseite | http://www.clinicaltrialssupply.com/Event.aspx?id=628228&MAC=DL | | | | | 4.CORE Summit — 2nd China Outcomes Research and Evidence Based Medicine Summit | | Termin | 29. Mär 2012 → 31. Mär 2012 | [ID=434393]  | | Ort | Shanghai, China | | Zusammenfassung | CORE Summit is the only venue in China that?s dedicated to outcomes research, comparative effectiveness research, health technology assessment, value based health management, and e-Health. It provides a platform for stake holders of government, industry, and medical community to share their vision and evidence on how to integrate population based clinical research into evidence based healthcare. | | Themen | outcomes research, real world research, value based healthcare, personalized medicine, evidence based medicine, registry, electronic medical record, electronic data capture, computer based medical education, cost effectiveness, observational clinical trials, comparative effectiveness research | | Webseite | http://www.coresummit.org | | Verwandte Fachgebiete | Medizin (allgem.) | | | | | 5.Vaccines China 2012 | | Termin | 23. Apr 2012 → 26. Apr 2012 | [ID=450246]  | | Ort | Shanghai, China | | Zusammenfassung | IBC's 4 th Vaccines China 2012 is timely and has been researched with the industry to provide the most comprehensive event focused on vaccines development through to manufacturing. Good manufacturing practices and strategies will be reviewed, alongside potential block-buster technologies and R&D projects. This conference is co-located with the 7 th annual China Pharmaceutical R&D Summit and 3 rd annual Biosimilars Asia conference to maximize cross-learning, partnering and networking opportunities with biopharma and related industries. | | Themen | viral, virology, bateria, virus, vaccine, R&D, pharmaceutical manufacturing, SFDA, WHO, biosimilar, biopharma, bioprocessing, upstream, downstream | | Webseite | http://vaccineschina.com/ | | Kontakt | Tel.: (6565082401/ (+86) 21 2326 3680 (China)); Email: rita.parasurum@ibcasia.com.sg | | Verwandte Fachgebiete | Biotechnologie | | | | | 6.Biosimilars Asia 2012 | | Termin | 23. Apr 2012 → 26. Apr 2012 | [ID=457966]  | | Ort | Shanghai, China | | Zusammenfassung | IBC?s 3rd Annual Biosimilars Asia 2012 is the largest and most anticipated meeting of its kind in Asia. Attended by biosimilars, innovators, generics and biopharma alike, the unique mix of attendees from all over the world will share, their experiences and opinions about the future of biosimilars. Tough questions, will be answered and positions will be challenged but all will walk away bristling, with ideas, opportunities and be more informed. Biosimilars Asia 2012, continues to deliver a quality of speakers and discussions unmatched in Asia. | | Themen | biosimilars, generics, vaccines, cell development,pharma regulations, FDA guidelines | | Webseite | http://www.biosimilarsasia.com/ | | Kontakt | Rita Parasurum; Tel.: ((+86) 21 2326 3680 (China) / (+65) 6508 2401 (All regions)); Email: rita.parasurum@ibcasia.com.sg | | | | | 7.ChinaBio® Partnering Forum 2012 | | Termin | 23. Mai 2012 → 24. Mai 2012 | [ID=453298]  | | Ort | Suzhou, China | | Veranstalter | EBD Group | | Webseite | http://www.dushulakehotel.com | | Kontakt | Mr Philipp Dormeier, Isartorplatz 4 Munich 80331 Germany | | | |
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Stand vom 03. Januar 2012
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