Perfil of Neha

Perfil of:
Neha
Member since 2023

User Type: Particular
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Province: Andhra Pradesh
City: Hyderabad

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Clinical research institute in hyderabad
. Medical Writing training and Regulatory Affairs course. We offer clinical research Certification Program also offers Clinical research Job Opportunities as Clinical Research Associate and Clinical Trials Associate. For CRA Training program the candidate should have B.Pharmacy,M.Pharmacy,Life Sciences ,Microbiology,Biotechnology,Chemistry. BPT,BDS and BHMS Also eligible for Clinical Research training program. For B.Pharmacy and M.Pharmacy the pharmacovigilance course is best suitable course. The pharmacovigilance training in hyderabad at gratisol imparts both theoretical and Practical with hands on experience on Argus database and MedDRa Medical browsers thus the reason gratisol is considered as the best pharmacovigilance institutes in hyerabad within the Pharmaceutical, Biotechnology and Medical Device industries to both experienced professionals and entry level candidates. The Clincal Data Manamgent Training offered fall into the broad categories of Recruitment Solutions, Temporary Staffing, Outsourcing, Consulting, Application Training in Clinical Data Management course (Oracle Clinical, Oracle Inform/Central Designer), Pharmacovigilance (Oracle Argus Safety Database, Oracle AERS), CDISC SDTM & SAS to aspirants of Clinical Research Industry. We successfully help some of the top Pharmaceutical, Biotechnology and Medical Device organizations from around the world to recruit high caliber experienced & trained professionals. The Pharmaceutical & Clinical Research Industry, worldwide is facing a huge shortage of trained manpower resources. With a View to fill this gap between the demand & supply of trained manpower and to help Pharmaceutical & Clinical Research industry to move on the fast track Gratisol Labs offers cutting-edge packaged and customized corporate training programs. In addition, Gratisol Labs has developed a tailored training division. Gratisol Academy of Clinical Research to provide Training, Internships, & Educational programmes that are designed to develop careers for clinical research professionals in Clinical Data Management, Pharmacovigilance & SAS. The focus of the lectures will be mainly on the following topics: » History and over view of pharmacovigilance » Introduction and responsibilities: USFDA, EMA and CDSCO » Pharmacovigilance in India » Clinical Development process » Different phases of clinical Trials » Adverse events and its types » Drug Safety in clinical trials and post marketed drugs » Different sources of Adverse events reporting » Different types of AE reporting Forms » Expedited reporting and its timelines » Different departments working on Pharmacovigilance » Roles and responsibilities of case receipt unit » Roles and responsibilities of Triage unit » Four factors for the reportable case » Seriousness criteria of adverse event » Expectedness or Listedness of adverse event » Causality assessment of the adverse event » Introduction to safety databases and different types » Importance and procedure of duplicate check » Case booking or initiation » Introduction to MedDRA and WHODD » Narrative writing » Case quality check, Medical review and its submission. » The Qualified Person for Pharmacovigilance (QPPV) in the European Economic Area » PSUR and its submission timelines Practical Training will be also provided on Safety Database on the following topics: » Data Entry » Case Processing » MedDRA & WHODD coding Gratisol Labs Advantages: » Oracle Argus Safety Database - Latest Production Version 7.0 » 4 months internship available after training » Own CRO live projects » Highest Placement record across all training institutes » Industry SOPs based training » Trainers with minimum 5 years experience » 24 hours access to application lab Course Timings 10:00-11:00 Am Trainer Information Industry Experts from Novartis, Parexel, TechMahindra, Infosys, HCL, MakroCare, Aurobindo Pharma, Natco Pharma
Hyderabad
Other Services - Hyderabad
May 24,

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