Vita Research Solutions
Vita Medical Center & Research Solutions, Inc. offers investigational site Research Services for all Phases of clinical trials. Our experience team provides expertise that allows personalized and flexible research services such as: Regulatory Affairs, IRB Submission, Inform Consent Form (ICF) writing and negotiation guidelines, Protocol design and writing, Source Documents writing, Adverse Event writing , Project management, Quality Control/Quality Assurance , Data management, eCRF data management.Vita Research Solutions Inc
Here are some terms you may encounter when you are browsing Vita Research Solutions websites:
Documentation: All records, in any form (including without limitation written, electronic, magnetic, and optical records, and scans, x-rays, and electrocardiograms) that describe or record the methods, conduct, and/or results of a trial, the factors affecting a trial, and the actions taken or omitted.
Clinical Trial / Study: Any investigation in human subjects intended to discover or verify the clinical, pharmacological, and/or other pharmacodynamic effects of an investigational product(s), and/or to identify any adverse reactions to an investigational product(s), and/or to study absorption, distribution, metabolism, and excretion of an investigational product(s) with the object of ascertaining its safety and/or efficacy. The terms clinical trial and clinical study are synonymous.Vita Research Solutions Inc
Vita Research Solutions:European Medicines Agency (EMEA): A decentralised body of the European Union with headquarters in London. Its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. The EMEA coordinates the evaluation and supervision of medicinal products throughout the European Union. The Agency brings together the scientific resources of the 25 EU Member States in a network of 42 national competent authorities. It cooperates closely with international partners, reinforcing the EU contribution to global harmonisation.
Source Documentation: Location where information is first recorded including original documents, data and records.
For more in formations please check the following articles: Vita Research Solutions website, Vita Research Solutions Inc blog and Vita Research Solutions news feed...
Vita Medical Center & Research Solutions, Inc. offers investigational site Research Services for all Phases of clinical trials. Our experience team provides expertise that allows personalized and flexible research services such as: Regulatory Affairs, IRB Submission, Inform Consent Form (ICF) writing and negotiation guidelines, Protocol design and writing, Source Documents writing, Adverse Event writing , Project management, Quality Control/Quality Assurance , Data management, eCRF data management.Vita Research Solutions Inc
Here are some terms you may encounter when you are browsing Vita Research Solutions websites:
Documentation: All records, in any form (including without limitation written, electronic, magnetic, and optical records, and scans, x-rays, and electrocardiograms) that describe or record the methods, conduct, and/or results of a trial, the factors affecting a trial, and the actions taken or omitted.
Clinical Trial / Study: Any investigation in human subjects intended to discover or verify the clinical, pharmacological, and/or other pharmacodynamic effects of an investigational product(s), and/or to identify any adverse reactions to an investigational product(s), and/or to study absorption, distribution, metabolism, and excretion of an investigational product(s) with the object of ascertaining its safety and/or efficacy. The terms clinical trial and clinical study are synonymous.Vita Research Solutions Inc
Vita Research Solutions:European Medicines Agency (EMEA): A decentralised body of the European Union with headquarters in London. Its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. The EMEA coordinates the evaluation and supervision of medicinal products throughout the European Union. The Agency brings together the scientific resources of the 25 EU Member States in a network of 42 national competent authorities. It cooperates closely with international partners, reinforcing the EU contribution to global harmonisation.
Source Documentation: Location where information is first recorded including original documents, data and records.
For more in formations please check the following articles: Vita Research Solutions website, Vita Research Solutions Inc blog and Vita Research Solutions news feed...