Samreen Randhawa Email & Phone Number

Canada

Canada

- Implementing and supporting operational decisions as determined and instructed by senior management.- Active member of SOP Review. Committee , Quality training and processes etc- Ensuring Accurate dispensing of prescription drugs is being done .- Maintenance of pharmacy Inventory .- Active participation in office meetings and proposals- Effective Drug Handling and Quality assurance: reduced error rate by 5% by helping in formulation of QA strategies for error minimization- Assist in writing internal SOPs and Working Instruction Guidelines (WIG) to streamline and formalize processes of day to day pharmacy operations

Ontario, Canada

Trained on both Healthwatch and Healthwatch DeltaHandling customer prescription pick upAssisting with cashier responsibilities as required in the PharmacyGood hands-on experience in packaging blisters/compliance packsCompounding oral and topical dose form.Accurate dispensing prescription medications

- Experienced Pharmacovigilance professional having worked in triage of all potential SAEs for expedited reporting, Data entry of reports (AERs) electronic (SAE) into a safety database/tracking system according to compliance with SOP/protocol.- Involved in importing all SAE documentation into safety database follow-up generation and performing query management , into the safety database.Database verifications for similar SAEs.- Handling incoming Adverse Events and access quality, providing internal feedback and training to maintain quality and compliance to regulatory timelines.- Preparing regulatory reports, including CIOMS I/MedWatch forms and/or line listings as needed for safety report preparation to competent authority.Involved in Quality checking various safety activities including data entry of patient information, processing of Adverse Events (AEs)/Endpoints according to Standard Operating Procedures (SOPs), and Project specific safety plans.- Handled tracking and management of line listings, Case Report Forms (CRFs), clinical data flow, SUSAR submissions and queries as required.- Familiar with international drug safety regulations (including ICH guidelines on safety and efficacy, US FDA guidelines, Health Canada guidelines,CIOMS, New EU PV legislation). Developing and reviewing departmental safety procedures (SOP), working instructions (WI) and templates. - Trained in report writing, coordination, medical writing and Periodic Benefit Risk Evaluation Reports (PBRERs), DSUR, Periodic Adverse Drug Experience Reports (PADERs), Addendum to Clinical Overviews (ACOs) and Semi-Annual Safety Reports.- Trained and mentored subordinates in various activities of SAE reporting and submission

Amritsar,Punjab India

• Drug dispensing• Prescription handling• Patient counseling

Advanced International Pharmacovigilance And Argus Safety Certification (Apvasc), A+

Applied Clinical Research Certificate, Clinical Research, A+

Certified Clinical Research professional

Master'S Degree, Pharmacy

Master'S Degree, Pharmacology

Bachelor Of Pharmacy - Bpharm, Pharmacy