Mohammad Iftakhar Email & Phone Number

Delhi, India

New Delhi Area, India

India

Medical and scientific Pharmacovigilance review of: -Literature Reports, Clinical trial reports, Clinical Trial (Serious) Adverse Event Reports -Post-marketing ADR reports -Case files, narratives, coding, causality and expectedness assessment • Analysis of Adverse Event Reports during on-going surveillance and signal detection, including independent analysis of safety risks • Writing of safety section, including PSURs, • Provide medical guidance to Safety Staff during the case… Show more Medical and scientific Pharmacovigilance review of: -Literature Reports, Clinical trial reports, Clinical Trial (Serious) Adverse Event Reports -Post-marketing ADR reports -Case files, narratives, coding, causality and expectedness assessment • Analysis of Adverse Event Reports during on-going surveillance and signal detection, including independent analysis of safety risks • Writing of safety section, including PSURs, • Provide medical guidance to Safety Staff during the case processing cycle • Learning to participate in Proposal Development Teams (PDTs) for client bid meetings • Maintain up-to-date knowledge of projects by attending Professional Society Meetings • Provide medical safety expertise to client per request • Provide medical safety expertise and training to other personnel, as required. • Maintain a current medical license • Keep current with professional and Pharmacovigilance regulations and knowledge • Accommodate Pharmacovigilance timelines through flexible approach to working hours Show less

Chennai Area, India

Medical reviewing of safety data, literature, and any other source and draw conclusions from safety reports, clinical reports, proficiency in medical report writing and safety standards. Clinical Review of all cases - serious and non-serious from different sources in different therapeutic areas.Responsibilities/Authorities :- Reviews and verifies appropriate selection of adverse events from source documents, appropriate code for each adverse event and accuracy of label assessments… Show more Medical reviewing of safety data, literature, and any other source and draw conclusions from safety reports, clinical reports, proficiency in medical report writing and safety standards. Clinical Review of all cases - serious and non-serious from different sources in different therapeutic areas.Responsibilities/Authorities :- Reviews and verifies appropriate selection of adverse events from source documents, appropriate code for each adverse event and accuracy of label assessments for each adverse event. - Provides a medical evaluation comment for all serious spontaneous, unlisted adverse events and serious related events from studies and solicited adverse events- Provides assessment(s) for study cases and solicited reports.- Reviews the source document to assure relevant information pertaining to the case is appropriately entered into the narrative.-Review and assessment of proper MedDRA coding of events, WHO coding of drugs, proper selection of suspect drugs. Show less

Teaching & training of medical & dental graduate students in clinical pharmacology along with there assessment through examination. Research work related to various field of pharmacology.

Md (Pharmacology), Clinical Pharmacology

Mbbs, Medicine & Surgery

Senior Secondary (10+2), Botony, Zology, Physics, Chemistry, Maths, English

10, Maths, Science, Social Science, English, Hindi