Explore the World of Pharmacovigilance and Regulatory Affairs
A Free Webinar on Career Opportunities
Introduction: Welcome to an exciting opportunity to delve into the world of Pharmacovigilance and Regulatory Affairs! Join us for a free, information-packed webinar where we will explore the vast career opportunities in these fields. Led by industry expert Mayuri, this one-hour webinar will provide valuable insights, practical advice, and guidance for those interested in pursuing a career in Pharmacovigilance and Regulatory Affairs. Whether you’re a recent graduate, a professional looking to switch careers, or simply curious about these industries, this webinar is for you!
Key Topics to be Covered:
- Introduction to Pharmacovigilance and Regulatory Affairs
- Importance of Pharmacovigilance in Drug Development
- Role of Regulatory Affairs in the Pharmaceutical Industry
- Career Paths and Opportunities in Pharmacovigilance and Regulatory Affairs
- Skills and Qualifications Required for Success
- Training and Education Programs Available
- Industry Trends and Future Outlook
- Q&A Session: Get your questions answered by Mayuri
Who Should Attend:
- Students and recent graduates interested in the pharmaceutical industry
- Professionals looking to transition into Pharmacovigilance and Regulatory Affairs
- Researchers and scientists seeking to expand their knowledge in drug safety and regulatory compliance
- Career counsellors and advisors guiding individuals in their career choices
Why Attend:
- Gain a comprehensive understanding of Pharmacovigilance and Regulatory Affairs and their significance in the pharmaceutical industry.
- Explore the diverse career paths and opportunities available in these fields.
- Learn about the skills, qualifications, and training necessary to excel in Pharmacovigilance and Regulatory Affairs.
- Get expert advice from Mayuri, an industry insider with extensive experience.
- Network with like-minded individuals and professionals in the field.
- Get your burning questions answered during the Q&A session.
Registration: To secure your spot for this free webinar, please visit. Hurry, as spaces are limited!
Don’t miss out on this exclusive opportunity to explore the world of Pharmacovigilance and Regulatory Affairs and uncover exciting career prospects. Join us for an engaging and informative webinar led by industry expert Mayuri. Take the first step towards a rewarding career in the pharmaceutical industry. Register now to secure your spot and mark your calendar for this not-to-be-missed event!
For any queries or further information, please contact us at +91 8480003645.
Date
- Jun 03 2023
- Expired!
Time
- 11:00 am - 12:00 am
Local Time
- Timezone: America/New_York
- Date: Jun 03 2023
- Time: 1:30 am - 2:30 pm
Cost
- Free
Location
- Online
Speaker
Mayuri Roy SinhaPV Trainer, Mentor For Academic & CorporatesExecutive Summary
Mayuri Roy Sinha has 13 years of Pharmacovigilance experience, including 12 years of training. She has worked on multiple client projects and worked as Manager in Pharmacovigilance, where she handled multiple teams performing time-bound activities. She has independently handled both clinical trials as well post-marketing projects. Due to her passion for Training she has been involved with training activities throughout her career and has been a trainer for both new joiners as well as for experienced team members, including Pharmaceutical Clients.She is currently working as Freelancer Pharmacovigilance Trainer with multiple academic and corporate sectors. She is an NIIT Certified trainer. In her current role, She is part of both academic and corporate training, writing, and consultancy services in the pharmacovigilance domain. She understands the requirements of the organization and the candidates before imparting training. She is involved in content writing, course designing, conducting an assessment, interview preparation, practical classes and project work in line with work done in the Industry.
Training ExpertiseShe delivers training on Pharmacovigilance Topics, Practical Work, Assessment, Safety Database, MedDRA Dictionary and doubt sessions for students. She also conducts technical interview mock sessions where She interacts with students and evaluates the level of clarity. Candidates can best utilize her professional experience to prepare themselves for Industry. She has handled multiple batches of both online and classroom sessions. She was a Project guide for BITS Mesra University Students in their final year Pharmacovigilance Project & handled 50+ batches so far.
Technical ExpertiseShe has expertise in Pharmacovigilance Project Work, Handling various Individual case safety report processing and team management. She was extensively involved in Compliance management for Pharmacovigilance team, with expertise in audit handling, and training management.
Projects handled:
ICSR Team Management & Training: ICSR team management as per the compliance & quality, Compliance management for the partner company SLAs, Regulatory Submission, SOP preparation & review, safety database validation, handling data migration projects, Client meeting to identify the need for opportunity and training for performance enhancement, performance review (appraisals) of the team members, Handling end to end PV operation for clinical trial actives included but not limited to literature screening, regulatory site review.
ICSR Team Management & Training: Pharmacovigilance Project guide for University students, Safety database training, PV theoretical training for multiple batches, designing course syllabus, preparation of question paper, conducting the workshop, journal club, presentation, University Final exam paper evaluation.
Tools Stack
Pharmacovigilance Safety Database including Arisg, Argus, AERS, PvEdge, PvNet
MedDRA Dictionary
Rave EDC
