United Conference of Quality and Validation

Theme : The Novel and Contemporary Research in Quality and Validation

Webinar on Quality and Validation | April 8, 2021

About The Conference

On behalf of United Conferences, we are overwhelmed to welcome all the interested participants to attend “United Conference of Quality and Validation” Webinar Event on April 8th, 2021. This conference boats of a huge variety of Keynote presentations, plenary talks, Poster presentations and Career development programs.

United Conference on Quality and Validation 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 Quality and Validation. 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 Quality and Validation.

Who Can Attend

  • Deans, Directors, CEO of an Organization
  • Business Development Managers
  • Chief Scientific Officers
  • R&D Researchers from Biosimilar and Biologic Industries
  • PhD Scholars
  • Professors, Associate professors, Assistant Professors
  • Drug Development Discovery Companies
  • Association, Association Presidents and Professionals
  • Formulation and Pharma Manufacturing Companies
  • Business Entrepreneurs
  • Medical Software Developing Companies
  • Manufacturing Medical Devices Companies
  • Intellectual Property Attorneys
  • Noble laureates in Health Care and Medicine
  • Pharmacists
  • Bio-instruments and Bio-informatics Professionals
  • Research Institutes and members
  • Pharmacy Institutes

Why To Attend

  • 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
  • Quality without compromise
  • Highly organised and structured scientific programs

Key Takeaways

  • CME / CNE / CPE / CDE Credits
  • 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

Scientific Sessions


President & CEO at GK Pharmaceuticals CMO, Florida, United States


Conferences Agenda



Webinar Registration Charges

  • Speaker Registration 0 USD
  • Delegate Registration 79 USD
  • Student Delegate 50 USD
  • Virtual Exhibitor 599 USD
  • Poster Presentation (Student) 50 USD
  • Young Research Forum (PhD Students and PDF's) 100 USD
  • Video Presentation 50 USD
  • E-Poster (Highlighted in the Website) 50 USD

United Pharma Technologies Collaborations and Associations

Mayra Liz Guzman-Kaslow
President & CEO at GK Pharmaceuticals CMO
Florida, United States
Biography: Mayra Liz Guzman-Kaslow is the Chairman and General Manager of GK Pharmaceuticals Contract Manufacturing Operations "GK CMO PR", sister company of GK Regulatory Compliance Corporation in Jacksonville FL-USA.

"GK-CMO PR" is the first and only Pharmaceutical and Biotechnology company in Puerto Rico that have the technology and capacity to perform Contract Development and Manufacturing Operations for Biosimilars, Biologics, Drug Substances, and Solid Drug products at the same facilities.
Also, Mayra is President & CEO / Principal Partner of GK Regulatory Compliance Corporation USA who is responsible to support all the technical projects, operations and manages our Jacksonville, FL office, and project portfolio.

Mayra hold a Master of Science in, Thermodynamics and Materials Sciences Engineering from the University of Cincinnati, OH, and 2 Bachelor in Science, (1st) in Analytical Chemistry, and (2nd) in Chemical Engineering from the University of Puerto Rico -- Mayaguez Campus. With over 26 years of experience and in-depth knowledge of FDA, EMA, MHRA, WHOs, ANVISA, COFEPRIS, ANMAT, CFDA KFDA, TGA, INVIMA, PMDA, SFDA, KFDA, ISO9001, ISO13485, Canadian, ICH Guidance, and regulations.

Track record for consistently meeting goals and delivering a high level sustained performance, proven the ability to build strong customer/client relationships to include conducting vendor audits and contract manufacturing oversight.

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