United Conference of Pharmacy and Health Care Systems

Theme : Innovations in Pharmacy and Medicine towards Building a Better Global Health Care System

Webinar on Pharmacy and Health Care Systems | November 17, 2021

About The Conference

United Conferences welcomes all the interested participants to attend the “United Conference of Pharmacy and Health Care Systems” Webinar Event on November 17, 2021. This conference glorifies a huge variety of Keynote Presentations, Plenary talks, Poster presentations, Video Presentations, and Career development programs.

United Conference of Pharmacy and Health Care Systems set one’s sights 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 Pharmacy and Health Care Systems. It exposes Pharmaceutical Care & Health Systems, Pharmacist in Public Health Care, Health care and medical informatics, Preventive Medicine and Behavioral Health etc. United Conference of Pharmacy and Health Care Systems provides industry and investors a single event to learn about cutting-edge knowledge on technologies and start-up companies. 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 Pharmacy and Health Care Systems.

Our Most Valuable Keynote Speakers

Gail Trauco

Advisory Committee Member COVID-19 FDA, Principal CEO The PharmaKon LLC, USA

Sr. Director-Head Of Formulation And Manufacturing, Avomeen, United States

CEO & Co-Founder Nexus eHealth Formal regional Medical Director for J&J and Eli Lilly Novartis: Pharmacovigilance Lead

Chief Compliance Officer At Engrail Therapeutics | CEO At PDC Pharma Strategy, USA

Jim Hauske
Jim Hauske

President And Founder At Sensor Pharma, United States

Timur Güvercinci
Timur Güvercinci

Director, Head Of External Supply Quality Processes And Development Bei Merck Gruppe Global Quality, Germany

Ravi Kalyanaraman
Ravi Kalyanaraman, Ph.D.

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

Danielle Drachmann

Executive Director At Ketotic Hypoglycemia International, Committee Member At The European Health Parliament, Patient Representative At The European Medicines Agency, Rare2030 EURORDIS, Europe

Stephan O. Krause

Head Of Product Quality Group At AstraZeneca Biologics, USA

Marieke Meulemans

CEO GCP Central B.V.,Amsterdam, North Holland, Netherlands

Karmen Trzupek
Karmen Trzupek

Director, Clinical Trial Services At InformedDNA, United States

Detlef Behrens
Detlef Behrens

Managing Director And Co-Founder At Bay Pharma GmbH Greater Kiel Area, Germany

Mathew Cherian
Mathew Cherian

Director & Senior Fellow Pharmaceutical Development, Hospira, A Pfizer Company, United States

Qihan Dong

Director, Chinese Medicine Anti-Cancer Evaluation Program, Sydney Medical School The Faculty Of Medicine And Health, The University Of Sydney, Australia

Li, Fengzhi

Faculty Member At Roswell Park Comprehensive Cancer Center, Roswell Park Cancer Institute, USA

James T. O'Donnell
James T. O'Donnell

Pharmacologist Drug Expert, Associate Professor At Rush Medical College, United States

Gareme Ladds

CEO PharSafer Associates Ltd - Global Leaders In Drug Safety, United Kingdom

Avik Pal
Avik Pal

Founder & CEO, CliniOps, Fremont, California, United States

Liana Kasyan

Founder/CEO And Principal PV Consultant At ETL Pharmacovigilance Center Ltd. Armenia

Eluemuno R Blyden

Founder/CEO At Avril Biopharma, Inc., United States

Previous Keynotes

Amanda DeMarzo

Associate Director, Patient Access New Jersey, United States

Zina Kobbi
Zina Kobbi

CEO of AREMA, Nabeul Governorate, Tunisia

Orlaith Ryan
Orlaith Ryan

Chief Technical Officer Shorla Pharma, Ireland

Marieke Meulemans

CEO GCP Central B.V.,Amsterdam, North Holland, Netherlands

Eden Lord

Founder & CEO at My City Med, Founder of The Civitas Foundation, USA

Executive Director at Ketotic Hypoglycemia International, Committee member at the European Health Parliament, Patient Representative at the European Medicines Agency, Rare2030 EURORDIS, Europe

CEO & Co-Founder Nexus eHealth Formal regional Medical Director for J&J and Eli Lilly Novartis: Pharmacovigilance Lead

Liana Kasyan

Founder/CEO and Principal PV Consultant at ETL Pharmacovigilance Center Ltd. Armenia

EU QPPV, Head of QPPVs & Safety Consulting. Pharmacovigilance Director, Sweden

Penelope Przekop

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

Shereen Agwa

Country Safety Team Lead for South Africa and Sub Saharan Africa, Egypt

Dr. Preeti Patel

Drug Safety Associate, Sollers, United States

Dr. Dina Avery

Assistant Professor & Associate Scientist - University of Alabama at Birmingham, USA

Veronika Valdova
Veronika Valdova

Ilana Frishman
Ilana Frishman

Safety Director at Pluristem Therapeutics, Israel

Ongoing Keynotes

Huma Qamar

Senior Vice President, Head of R&D Program, FSD Pharma, Inc. USA

Hetal Shah

Pharmaceuticals & CROs - Independent Consultant & Founder-Director - MeWriT Healthcare Consulting, India

Gail Trauco

Advisory Committee Member COVID-19 FDA, Principal CEO The PharmaKon LLC, USA

Dr Lia Hunter

Director Clinnovate Ltd, south Croydon, England, United Kingdom

Galyna Malygina

Senior Project Manager, LLC OtiPharm® Data Pro

Rebecca Centko

Director of Project Management & Account Management, Regis Technologies, USA

Speakers

Sessions and Tracks

  • Pharmaceutical Care & Health Systems
  • Public Health Care and Preventive Medicine
  • Health care and Medical informatics
  • Womens Health Care
  • Preventive Medicine and Behavioral Health
  • Health Care and Infectious Disease
  • Nursing and Health Care
  • Psychological Health Care
  • Advanced Health Care Oncology
  • Clinical Pharmacology & Biopharmaceutics
  • Pharmacovigilance and Drug Safety
  • Obesity Health Disorders
  • Advanced Healthcare & Innovations
  • Pediatrics Health Care
  • Neuropharmacology Care
  • Advances in Pharmacological Research
  • Cardio Vascular Pharmacology health care
  • Clinical Pharmacology and drug discovery
  • Psychology and psychiatric Disorder Health Care
  • Pharmaceutical Analysis and Developments
  • Pharmaceutical Regulatory Science & Developments
  • Healthcare Patient safety
  • Research & Development in pharmacy
  • Health Care Statistics and Research
  • Preventive Medicine and Dermatology
  • Drug interactions and protocols

Virtual Exhibitors

ASTE Logo

ASTE Pharmaceuticals, Medical & Laboratory Supplies

TGMP Consulting

Webinar Registration Charges

  • Keynote/ Speaker Registration 249 USD
  • Speaker Registration 199 USD
  • Delegate Registration 129 USD
  • Student Delegate Registration 79 USD
  • Poster Presentation Registration 99 USD
  • Video Presentation Registration 99 USD
  • E-Banner Registration 99 USD

Who Can Attend

  • Managers, Directors, and VPs.
  • Pharmaceutical companies.
  • Hospitals, healthcare system & healthcare providers.
  • Health insurance companies.
  • Biotech companies
  • Medical device manufacturers.
  • Healthcare-related associations and foundations.
  • Industry influencers (solutions providers, educational organizations, government entities and venture capitalists).

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

Gail Trauco
Gail Trauco
Advisory Committee Member COVID-19 FDA, Principal CEO The PharmaKon LLC, USA
Biography: The PharmaKon LLC specializes in clinical pharmaceutical product development and trials. It is a 100% woman owned business led by its CEO/founder Gail Trauco, R.N., BSN-OCN. The PharmaKon partners with biopharmaceutical and biotech companies, investigators, site staff, lab and technology vendors, and regulatory authorities to reinforce patient safety and access throughout every phase of research. All play a part in delivering the quality data that can drive promising compounds forward.
For nearly 30 years, The PharmaKon’s dedicated government and public health services group has successfully delivered clinical research services to various agencies, contractors and nonprofits in both prime contractor and subcontractor capacities within full compliance of all federal contracting requirements. Its services have supported the organizations in conducting therapeutic, vaccine and medical device studies on a global scale across all trial phases and therapeutic areas.

The PharmaKon has a unique understanding and connection to rural healthcare and underserved communities by way of Trauco’s personal experiences growing up on a family farm in her native North Carolina. Despite challenges with generational grief and poverty, Trauco persevered through high school and college at University of North Carolina at Chapel Hill and then began a life and career of her own as an oncology nurse. Trauco worked for the Chief of Surgical Oncology at Duke University Cancer Cener, Dr. Hilliard Siegler, a pioneer in the field of immunotherapy in 1957, whom she credits for her foundation of knowledge about medicine.

A registered Oncology nurse, pharmaceutical trials expert, and long-time Patient advocate, Trauco has spent four decades helping patients navigate the sea of red tape in the American healthcare system. Based just outside Atlanta, she has gained a reputation as a fierce advocate for patient’s rights and for resolving some of the most difficult medical cases in the currently crippled healthcare industry. As a lifelong healthcare professional and frequent on camera expert, Gail Trauco is equal parts Gloria Allred, Erin Brokovich, and Nancy Grace…with a small twist of Dog the Bounty Hunter.

For more information about Gail Trauco and The PharmaKonLLC visit:
https://thepharmakonllc.com/
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.
Nashwa Nashaat
CEO & Co-Founder Nexus eHealth Formal regional Medical Director for J&J and Eli Lilly Novartis: Pharmacovigilance Lead
Biography: She has dedicated her career to improving the patients’ care and healthcare services. Inspired by the advancement in technology and her personal mission to serve patients, she has co-founded a company where the unmet patient’s needs drive the innovation for personalized technology-based solutions. In her role as a Chief Executive Officer and Co-founder for Nexus eHealth, she is committed to being a catalyst in the adoption of precision medicine through the Technology Enabled Connected Care solutions and building the healthcare technology capabilities, especially in the Middle East and Africa.
Prior to founding Nexus eHealth, being a physician; with PhD in Pediatric Oncology/Hematology, she devoted her passion to improve cancer patients’ lives and affordability of medicine by working with different global medical societies, NGOs and policy makers for more than 18 years. She has also worked for top multinational pharmaceutical, diagnostics and medical devices companies (Novartis, Eli Lilly and Johnson & Johnson) during the last 11 years where she took several global executive leadership roles in R&D, GxP auditing, medical affairs, patients advocacy and support programs, governmental affairs, business development, market access, healthcare policies and digital transformation strategies.

She was honored with 25 global awards for innovation, excellence and patient centricity. She authored more than 20 scientific publications. She serves as technical advisor and organizational leadership coach qualified by Glasgow university. She has been volunteering in different community services in Africa and a member in the Global Camper of Commerce and Industry (GCCI) that support the spirit of entrepreneurship. She is an Egyptian woman who constantly advocates the promotion of equality, diversity and inclusion & woman empowerment across the corporate world and the society as a whole.
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.
Biography: Executive director at Ketotic Hypoglycemia International. Her work started with the establishment of an international patient association where they are in close collaboration with national and international researchers, have written scientific papers and conducted research projects using a Citizen Science approach. Most recently, she entered the European Health Parliament and the European Medicines Agency as a Patient Representative for patients with rare hypoglycemia diseases. Furthermore, she have been working for EURORDIS (European Organization for Rare Diseases) to develop recommendations for Europes' rare disease policy in the Rare2030 project.
Stephan O. Krause
Stephan O. Krause
Head of Product Quality Group at AstraZeneca Biologics, USA
Biography: Stephan Krause, PhD, is currently Quality Director and PQL Team Leader in Development Quality, AstraZeneca Biologics. He is a results-driven leader with 20 years of technical, managerial, and executive experiences for quality and technical functions within global operations. He is a frequent conference presenter and author and has won multiple industry awards for his publications and leadership in improving industry best practices. Stephan was invited by FDA several times to present an industry perspective to the agency on relevant current topics. He is a member of PDA’s Board of Directors and is co-chair of AMTP Advisory Board and a member of the Advisory Board for Biopharmaceuticals and Regulatory Affairs/Quality.
Marieke Meulemans
Marieke Meulemans
CEO GCP Central B.V., Amsterdam, North Holland, Netherlands
Biography: She is a Founder and CEO of GCP Central since 2012 with over 15 years of experience within the clinical research world, and is the driving force behind the company vision.

Expertise:
•Development of practice-based and effective online GCP training for clinical research professionals.
•Setup and implementation of Learning Management Systems.

Specialties: eLearning development ; online GCP training; training needs analysis; process improvement; training management; blended learning; Good Clinical Practice; Clinical research rules & regulations; Wet Medisch Wetenschappelijk Onderzoek (WMO) training
Biography: Dr Dong was trained as a Physician then pursued a research career after completing his PhD at the University of Sydney. He continued as a Fogarty Fellow at the National Institutes of Health, USA. On returning to Sydney, he was appointed as the Head of the Cancer Biology Group. Currently, he is Associate Professor and the Director of newly-established Chinese Medicine Anti-cancer Evaluation Program at the Medical School in University of Sydney. He has published 81 papers (3,800 citations) in journals with an average Impact Factor of 4.1. He has been the first or senior author on 70% of them. His team was the first to discover that in prostate cancer cells the expression of the native inhibitory gene of phospholipase decreased. This content has been published three times in "Cancer Research" and "Clinical Cancer Research", and has been included in the latest European edition of "Encyclopedia of Cancer".
Biography: Fengzhi Li became a faculty member at Roswell Park Comprehensive Cancer Center (legal name: Roswell Park Cancer Institute, the first cancer institution in the US history and is a US NCI-designated comprehensive cancer center) in 2001 after finishing his postdoctoral training in Dr. Dario C. Altieri’s laboratory at Boyer Center for Molecular Medicine, Yale Medical School where he focused his research on the characterization of the function and expression regulation of a newly discovered antiapoptotic protein named survivin (a novel member of the inhibitor of apoptosis protein family). In 2006 he has been promoted to Associate Professor of Oncology at Roswell Park. As a chief scientist, he leads his lab using the survivin gene as a target and biomarker for targeted drug discovery. He has transitioned his Roswell Park cancer research lab from basic to translational cancer research over the past decade. His current research interests focus on targeted anticancer drug discovery, development and mechanism of action (MOA) studies. His research has been supported through federal agencies (NIH/NCI, DOD) as well as other public/private foundations and partnerships. He has published over 80 publications (h-index, 47 and i10-index, 73) with a total citation of over 13,000 times. He is the editorial board members in several academic journals including J Exp Clin Can Res (2019 IF: 7.068), Am J Transl Res (2019 IF: 3.375) and Int J Mol Sci (2019 IF: 4.556). He is also the Chief Scientific Officer (CSO) of Canget BioTekpharma LLC (www.canget-biotek.com) and helps Canget to develop innovative targeted anticancer drugs (high efficacy with low toxicity) for benefiting cancer patients.
Biography: Graeme Ladds has worked in Global Pharmacovigilance and Medical Affairs for the last 30 years working with many top ten Pharma in senior positions. He has worked in all areas of Pharmacovigilance and has designed and improved many IT solutions to aid both Medical Affairs and Pharmacovigilance. Graeme is also an experienced GCP/PV auditor having audited many Companies globally as well as helping Companies in Regulatory Inspections. He now works in his CRO - PharSafer Associates Ltd
Liana Kasyan
Liana Kasyan
Founder/CEO and Principal PV Consultant at ETL Pharmacovigilance Center Ltd. Armenia
Biography: Founder/CEO and Principal PV Consultant at the ETL Pharmacovigilance Center Ltd., - Pharmacovigilance Instructor at the Open Education Office of the American University of Armenia, - Member of International Society of Pharmacovigilance (ISoP), - International Editorial Board Member for the Journal of Pharmacovigilance and Drug Research (JPADR), - Reviewer of Master Тheses at the Faculty of Public Health of Yerevan State Medical University, - Board Member of Armenian Association of Specialists in Evidence-Based Medicine (AASEBM), - Co-founder of “Do not Harm’’ Health NGO.
Huma Qamar
Huma Qamar
Senior Vice President, Head of R&D Program, FSD Pharma, Inc. USA
Biography: Huma Qamar is a Health care professional with more than 16 years of work experience in clinical medicine, surgery, pharmaceutical, Health Law, Oncology Research, patient centered outcomes research, Phase 1 trials, Women's Health, Sarcoma, Melanoma, Hematology, CART-19,Clinical Operations, Medicare Coverage Analysis, Prospective Reimbursement Analysis, Medical Affairs, Vendor Management, Good Clinical Practice (GCP), ICH, Fetal and Pediatric research, IND/IDE, Project planning, CRO, Medical Devices, Clinical Protocols, Flexible Schedule, Calibration,health outcomes research, public health, clinical research, regulatory affairs in research development, organizational delivery, Pharmacovigilance, mental health counseling, research project management, program planning and evaluation, clinical trial budgets and contracts, billing and compliance, epidemiology, electronic data capture (EDC), statistics, health marketing, information technology and business development in multiple therapeutic areas.Excellent leadership, management, interpersonal, presentation and communication skills. High degree of emotional intelligence with ability to connect with people and build strong cross-functional relationships, internally and externally.
Hetal Shah
Dr. Hetal Shah
Pharmaceuticals & CROs - Independent Consultant & Founder-Director - MeWriT Healthcare Consulting, India
Biography: Dr Hetal Shah, an expert medical writing professional by passion and profession; is currently the Founder - Director of MeWriT Healthcare Consulting.

Dr Shah is a PhD Pharmacologist with over 17 years of first-hand experience in the field of medical writing and clinical research project management. A gold medallist for her manifold academic achievements, she also has several national and international publications to her credit including book chapters, research papers and reviews.
An independent consultant with high standards for quality and work ethics, Dr Shah is extensively involved in developing integral regulatory documentation & publications for pharmaceuticals & research organizations.

As a medical writing expert, she takes full accountability for first-hand writing, editing and finalizing of submission-ready documents for various therapeutic areas. Her writing sphere currently ranges from preparation of clinical trial documents to clinical study reports; compilation of drug authorization dossiers to scientific publications for journals.

She is also an experienced trainer with practical approach to coaching, and independently conducts medical writing workshops customized for various topics and audiences’ needs. She is a member of the executive committee of All India Medical Writers Society (Under formation), member of Indian Society od Clinical Research, and an ex-member of the DIA Medical Writing group of India and ISMPP.

An accomplished professional herself, she effectively collaborates with medical experts, bio-statisticians, in-house and allied teams to ensure a complete, accurate, cost-effective, and timely solution for your medical writing needs, with the best of quality and ethics.
Dr Lia Hunter
Dr Lia Hunter
Director Clinnovate Ltd, South Croydon, England, United Kingdom
Biography: Dr Lia Hunter has over 25 years experience in the Pharmaceutical/ Biopharmaceutical Industry. She has held various positions including Research Chemist, Lecturer, Clinical Trial Administrator, Clinical Research Associate, Clinical Trial Auditor, Clinical Project Manager and Consultant. This expansive experience has developed skills and expertise such that she has overseen the progression of projects from the preclinical phase right through to market authorisation.
In 2015, Lia set up Clinnovate Ltd, a Clinical Research Consultancy, providing expertise to pharmaceutical and biopharmaceutical companies to facilitate clinical project delivery. In this capacity, Lia has successfully delivered trials within the timelines and to budget, whilst ensuring patient safety, data integrity and regulatory compliance is never compromised.

Lia has extensive experience leading key studies on high profile programmes for leading pharmaceutical companies, especially in Oncology, Gastroenterology and Infectious disease. Lia worked on a key programme for her client Takeda Pharmaceuticals in a Global position with oversight of the CRO Strategic Partner and associated Vendors and is Leading Clinical Operations Oversight at Biogen currently.
Galyna Malygina
Galyna Malygina
Senior Project Manager, LLC OtiPharm® Data Pro
Biography: An expert in the implementation and development of projects of various levels. In the IT industry since 2008, has extensive experience in other industries. Speaker of pharmaceutical forums, provide consultation to pharmaceutical companies in choosing IT products for automatisation business processes inside of the company.
Rebecca Centko
Rebecca Centko
Director of Project Management & Account Management, Regis Technologies, USA
Biography: Rebecca Centko is an Excellent communicator with a strong ability to manage business needs while delivering for clients. I have an ability to influence at all levels of the organization. I have a demonstrated history of leading a project management group with a strong understanding of the sales process, business needs, the drug development process, quality aspects, and cGMP manufacturing requirements. I can work within a team to identify and resolve problems quickly.

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