United Conference of Generic Medicine, Vaccines and Biosimilars

Theme : The Novel and Contemporary Research in Generic Medicine, Vaccines and Biosimilars

Webinar on Generic Medicine, Vaccines and Biosimilars | April 9, 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.

Keynotes

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

Sr. Director-Head of Formulation and Manufacturing, Avomeen, United States

Chief Compliance Officer at Engrail Therapeutics | CEO at PDC Pharma Strategy, United States

Ravi Kalyanaraman

Director, Global Analytical Science & Technology - Pharma & Forensics Bristol Myers Squibb, United States

Timur Güvercinci
Timur Güvercinci

Director, Head of External Supply Quality Processes and Development bei Merck Gruppe Global Quality, Germany

Wendi Young
Wendi Young

President at Triverity Laboratories Greeley, Colorado, United States

Speakers

Dhaval Surti

Heading QA, Emcure Pharmaceuticals Limited, India

Md. Saddam Nawaz

Head of Quality Assurance, ACI HealthCare Limited, Bangladesh

Elie Arslan

Manager, Technical QA and Document Control at Ajinomoto Bio-Pharma, United States

Majdi Ayoub

Quality & Validation Manager at Rieckermann GmbH Jordan

Dishant Sanghavi

Senior Manager - Global Quality and Compliance, Sun Pharma, India

Mohammad Refaat Khattab, Ph.D

Scientist at Texas A&M University - USA

Virtual Exhibitors

PRA Consultancy

Professionals Regulatory Affairs (PRA) Consultancy

ASTE Logo

ASTE Pharmaceuticals, Medical & Laboratory Supplies

Caldic

EMD Group

Webinar Registration Charges

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 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
  • 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

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.
Hashim Ahmed
Head of Formulation and Manufacturing at Avomeen. Wake Forest, North Carolina, United States
Biography: A pharmaceutical product development executive leader with wide experience in CMC/MS&T-product development-R&D expertise with in-depth diversified global technical and management experience. Expert in formulation/process/product development supply management; and quality assurance of pharmaceutical/consumer products. Over 26 years of experience in the United States in major, medium-to-small companies (Roche/Stiefel-GSK/Dr. Reddy's). Consumer Product Development and regulatory expert in a diverse portfolio of APIs and a wide range of dosage forms, with NDA/505b2/generic-ANDA experience.
In-depth experience in small and large molecules (proteins/peptides); orals (tablets, capsules [hard-soft gel]); controlled-modified release formulations; as well as/parenterals dosages. Expert in oral Liquids Emulsions-Suspensions, Lipids, Powders, Topicals, Transdermals, Ocular delivery, Intranasal, Aerosols. SKILLS: Proven Product Development/CMC/Regulatory Leader (26 years in the USA at different pharmaceutical technical and management capacities); currently managing general director at QLife the lead pharma company in Qatar.
Penelope Przekop
Chief Compliance Officer at Engrail Therapeutics | CEO at PDC Pharma Strategy
Biography: Penelope Przekop, MSQA, RQAP-GCP is the CEO of PDC Pharma Strategy, a consulting firm that focuses on strategic GxP regulatory and corporate compliance. She currently dedicates half of her time to serving as Chief Compliance Officer for Engrail Therapeutics, Inc. She has 30-plus years of broad and deep pharma industry experience and is known for her creative approaches to developing efficient quality management strategies that enable companies of all sizes to build upon their unique drug development history and strengths while ensuring compliance.
Penelope earned her B.S. in Biology from Louisiana State University and her M.S in Quality Systems Engineering from the Kennesaw State University. She is a frequent industry speaker and writer. She is the author of Six Sigma for Business Excellence (McGraw-Hill). Her upcoming book, 5-Star Career (Productivity Press, fall 2021), will relay how readers can apply the proven science of quality management to career development.

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