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United Conference of Regulatory Affairs
Theme : The Novel and Contemporary Research in Nanotechnology and Medicine
Webinar on Regulatory Affairs | July 14-15, 2021
About The Conference
On behalf of United Conferences, we are overwhelmed to welcome all the interested participants to attend “United Conference of Regulatory Affairs” Webinar Event on July 14-15, 2021. This conference boats of a huge variety of Keynote presentations, plenary talks, Poster presentations and Career development programs.
United Conference of Regulatory Affairs aims to bring together a significant number of leading academic scientists, researchers, and research scholars to exchange and share their experiences and research results on all aspects of Regulatory Affairs. It is a foremost integrative platform for researchers, educators, and practitioners alike to present and explore the latest innovations, trends, and concerns as well as practical challenges encountered, and solutions adopted in the fields of Regulatory Affairs.
Previous Keynotes
Professor of Joining and Welding Research Institute (JWRI), Osaka University, Japan
Chief Executive Officer at NanomediGene LLC, United States
Formulation Scientist, United States
Director/Professor of Nanotechnology & Regenerative Medicine & NanoRegMed Ltd, United Kingdom
Investigator & Quality Manager, Nanopharmacia Diagnóstica, Mexico
Nanomedicine Scientist, USA
Founding Chair, President/CEO and Institute Professor at International Institute of Medicine & Science
Ongoing Keynotes
Speakers
Heading QA, Emcure Pharmaceuticals Limited, India
Head of Quality Assurance, ACI HealthCare Limited, Bangladesh
Manager, Technical QA and Document Control at Ajinomoto Bio-Pharma, United States
Quality & Validation Manager at Rieckermann GmbH Jordan
Senior Manager - Global Quality and Compliance, Sun Pharma, India
Scientist at Texas A&M University - USA
Virtual Exhibitors
ASTE Pharmaceuticals, Medical & Laboratory Supplies
TGMP Consulting
Webinar Registration Charges
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Keynote/ Speaker Registration 199 USD
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Speaker Registration 149 USD
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Delegate Registration 99 USD
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Student Delegate Registration 50 USD
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Poster Presentation Registration 50 USD
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Video Presentation Registration 50 USD
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E-Banner Registration 50 USD
Who Can Attend
- Regulatory affairs professionals.
- Development and preparation of submissions.
- Newcomers, managers, or directors in the drug or medical device industries.
- Research and development.
- Quality assurance and control.
- Manufacturers and researchers who are responsible for ensuring the cybersecurity of their medical devices.
- Global manufacturers who are seeking to harmonize their manufacturing activities to comply with multiple country regulatory bodies.
- Medical device stakeholders who want to find online resources that explain pre-market and post market regulatory framework for medical devices
- Regulatory affairs professionals seeking to submit new or novel medical device regulatory submissions, including premarket notifications (510(k)s) and De Novos.
- Manufacturers and regulatory affairs professionals seeking to enhance their knowledge about the FDA Quality System (21 CFR 820) and applicable subsystems
Why Choose Us
- Global & Local Expertise
- Prospective Attendees
- Larger worldview of the profession
- We’re passionate about what we do
- We focus on your career growth
- Transparency in Communication
- Open gateway towards INNOVATION
- Strong sense of identification
- Quality without compromise
- Highly organised and structured scientific programs
Key Takeaways
- Professional Worldwide
- International Recognition of Researchers
- Knowledge into Asset
- Cognizance of leading Cutting – Edge technologies
- Publication of Abstracts in preeminent supported journals
- New Accomplishments with Edu – tech ideas
- Exposure to the upcoming business trends
- Free access to our forthcoming International events
- Certificate of presentation with International signatories
United Pharma Technologies Collaborations and Associations
