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Clinical Trial Regulations With ICH GCP E6 R2 Workshop
17-19 Sep 2019
Leonardo Hotel Amsterdam Rembrandtpark, Netherlands
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Clinical Trial Regulations With ICH GCP E6 R2 Workshop
Description
Topics
EU Annex 13
GCP requirements for the sponsor related to IMP
Distribution to sites
Handling of IMP at sites
Handling of IMP temperature deviations and complaints
Transfer of IMP between sites
Who should Attend
Biotech companies
Clinical Research Organizations
Large to small Pharmaceutical companies
Clinical Research Services Suppliers
Non-Commercial Research Organizations
Past Events
Clinical Trial Regulations With ICH GCP E6 R2 Workshop - 17-19 Sep 2019, Leonardo Hotel Amsterdam Rembrandtpark, Netherlands
(86788)
Important
Please, check "Clinical Trial Regulations With ICH GCP E6 R2 Workshop" official website for possible changes, before making any traveling arrangements
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Health & Medicine:
Healthcare, Medical laboratories, Medical technology, Pharma
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