Mohd. Asif Zawed Email & Phone Number

Delhi, India

Gurugram, Haryana, India

1. Designing and implementation of patient support program in alignment with organization or client..2. Provide strategies for continued growth of PSP focused on addressing patient needs while balancing compliance including communication strategy4. Support review and development of patient support materials including program blueprints.5. Ensuring internal.

Gurugram, Haryana, India

Gurugram, Haryana, India

• Ensuring the correctly identification of AE information received over the call/email/any document.
• Reviewing the Adverse event form before forwarding them to the Drug Safety Unit(DSU).
• Provide feedback to health coaches [Calling team] on a case-by-case basis afterreviewing the cases.
• Prepare monthly Management Information System (MIS) reports summarizing allreported AEs to the DSU.
• Ensure receipt of AER numbers from the DSU and follow up with reminders ifnecessary.
• Coordinate with the DSU to resolve any outstanding issues related to AE reporting.

Ministry Of Health And Family Welfare Of India

• Jr. Pharmacovigilance Associate [Jan-21 to July-21] at National Coordination centre,Pharmacovigilance programme of India, Indian Pharmacopoeia Commission (IPC)Ministry of health and family welfare (MoHFW), Gov. of India.
• Managing 15 adverse drug reaction monitoring centre (AMC), this is recognised underIndian pharmacopoeia commission. Responsible to manage all activities of PVregulatory affairs at AMCs.
• Processing of Individual case safety reports (ICSRs) And periodic safety update reports(PSURs)_ received from marketing Authorization holder (MAH)
• Assisting in Updating or amending the PV guideline for MAH
• Performing the assigned task with respect to the WHO collaborating centre related toregulatory affairs.
• Assisting in effective implementation of Pharmacovigilance guideline for MAH

New Delhi Area, India

• Clinical Trial Management, Subject Level Data Review, Patient Recruitment, Source Documentation, CRF Queries.
• Trained on ICH-GCP, Schedule Y, New Drug & Clinical Trial Rule 2019.
• In depth knowledge of drug development and clinical trials (phase I to IV).
• Knowledge and understanding of ethics review process.
• Standard Operating Procedure (SOP) & Good Documentation Practice (GDP).
• Informed Consent (ICF) Process.

Sector 5 IMT Manesar, Gurgaon Haryana.

C-46 Noida Sect -62 Utter Pradesh.

As a Project trainee in clinical pharmacological unit Jubilant Genrics Ltd.

Bachelor'S Degree In Pharmacy, Department Of Pharmacy, New Delhi

👉Hands on various laboratory equipment like Freeze Dryer, Dissolution Apparatus (USP-II), Disintegration Apparatus (Electrolab).

Master'S Degree In Pharmacy, Pharmacology

👉Animal handling and various routes of drug administration, observed anti-inflammatory action, muscle relaxant properties and bioassay.