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Worksuremedphar04 Jul, 2017Health
WorkSure® a first medical service KPO in India, works as medical knowledge partner to various health care industries. WorkSure® a first medical service KPO in India, works as medical knowledge partner to various health care industries.
Worksuremedphar04 Jul, 2017Health
According to WHO “Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention. According to WHO “Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention
Worksuremedphar04 Jul, 2017Health
Clinical research determines the safety and efficacy of medications, devices, diagnostic products and treatment regimens discovered. Clinical research determines the safety and efficacy of medications, devices, diagnostic products and treatment regimens discovered
Worksuremedphar04 Jul, 2017Health
WorkSure, Pharmaceutical & Healthcare Consultancy, take this opportunity to introduce “Facilitating Medical Research Communication (FMRC) WorkSure, Pharmaceutical & Healthcare Consultancy, take this opportunity to introduce “Facilitating Medical Research Communication (FMRC)
Worksuremedphar04 Jul, 2017Health
Clinical research team works closely with the clinical development team for planning and organizing clinical trials. Clinical research team works closely with the clinical development team for planning and organizing clinical trials.
Worksuremedphar04 Jul, 2017Health
WorkSue® Medical Affairs Management Services to sales & marketing, clinical trials, pharmacovigilance, regulatory and legal departments. WorkSue® Medical Affairs Management Services to sales & marketing, clinical trials, pharmacovigilance, regulatory and legal departments.
Worksuremedphar04 Jul, 2017Health
WorkSure® Documentation serves as a backbone for successful conduct of a clinical study or scientific research. WorkSure® Documentation serves as a backbone for successful conduct of a clinical study or scientific research.
Worksuremedphar04 Jul, 2017Health
A Clinical Trial Application (CTA) is submitted to regulatory authority to seek approval for conduct of a clinical trial in India A Clinical Trial Application (CTA) is submitted to regulatory authority to seek approval for conduct of a clinical trial in India
Worksuremedphar04 Jul, 2017Health
Clinical Trial Authorization (CTA) is mandatory to conduct clinical trials in humans. CTA can only be obtained after submission of a group Clinical Trial Authorization (CTA) is mandatory to conduct clinical trials in humans. CTA can only be obtained after submission of a group
Worksuremedphar04 Jul, 2017Health
Risk Evaluation and Mitigation Strategies (REMS for US FDA) and Risk Management Plan (RMP for EU) are two main risk management strategies Risk Evaluation and Mitigation Strategies (REMS for US FDA) and Risk Management Plan (RMP for EU) are two main risk management strategies
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