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PROCESS VALIDATION & CONTINUED VERIFICATION

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Master Planning * Risk * Statistics * Change Control * Documentation * CPV

March 25 - March 27

Philadelphia, United States



Process Validation & Continued Process Verification (CPV)

 

Process Validation is the backbone of all validation and is always under FDA regulatory scrutiny. KENX is excited to announce the definitive process validation and continued process verification conference of 2019. This event gives you the tools and technology needed to create, deploy and maintain best practices through all three stages of validation. Come to Philadelphia this spring and align with best-in-class case studies that impress FDA investigators and make an immediate impact for your organization and professional career.

 

Top 10 Reasons to Attend:

  • Walk through a risk-based implementation case study
  • Master the Validation Master Plan (VMP)
  • Establish a compliant Continued Process Verification (CPV) process
  • Uncover the top 5 challenges
  • Leverage technology transfer and engineering studies
  • Discover a Quality by Design (QbD) approach
  • Process Performance Qualification (PPQ) – Select the optimal sampling plan
  • Develop a gap analysis checklist for your program
  • Understand how to use statistics in process validation
  • Learn an effective approach for combination products

 

Personnel in the Following Environments Should Attend:

  • Validation
  • QA/QC
  • Engineering
  • Regulatory Affairs
  • Compliance
  • Manufacturing
  • Laboratory

 

This event is also appropriate to business development and sales managers that offer innovative solutions for change control, risk management, statistics and validation.

 

Click Here to View the Agenda-At-A-Glance

 

 

Agenda

  • 12:00
    Conference Registration
    Coffee & Lite Snacks On-the-Go
  • 1:00
    1:00 Chairperson’s Opening Remarks
  • 1:15
    Breaking News - FDA Releases Data Integrity and Compliance With Drug CGMP Questions and Answers Guidance for Industry
    Chris Wubbolt, Principal, QACV Consulting, LLC
  • 2:00
    Tips on Handling Data Integrity and Validation Inspections – An FDA Perspective
    Karyn M. Campbell, Director, Investigations Branch II, Division of Pharmaceutical Quality Operations, U.S. Food and Drug Administration (FDA)
  • 2:30
    Staying Ahead of the Validation and GMP Regulatory Curve through Warning Letter Knowledge
    Erik Muegge, M.S., Manager Operations Quality, Abbott Laboratories
  • 3:00
    Afternoon Networking Refreshment Break
  • 3:30
    Overcome the Top Five Validation Challenges
    Connie Hetzler, Global Head of Validation, Alcon Laboratories
  • 4:00
    Implementation of a Risk-based Cleaning Validation Management System
    Parsa Famili, President & CEO, Novatek International
  • 4:30
    A Systematic Approach for a Knowledge Management Model
    Robert J. Wherry, Head – R&D Data Systems QA & Compliance, Takeda
  • 5:00
    Temple University Scholarship Award & Welcome Reception
  • Close of Day One
  • 7:00
    Coffee and Lite Breakfast
  • 7:30-8:15
    Select Between Knowledge Exchange Sessions (1-4)
  • (1)
    Documentation Requirements for Successful Validation
    Gamal Amer, Ph.D. Principal, Premier Compliance Services
  • (2)
    Qualification of Water Systems, Clean Steam Systems & Process Gasses
    Patrick Mullin, Senior CQV/QAV Consultant, DPS Group Global
  • (3)
    Strategies to Move to Electronic Systems
    Lelia Scott, Senior Director Global Quality Systems, Charles River Laboratories
  • (4) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Data Integrity – Navigating the Maze of Regulations
    Kevin Martin, Managing Partner, Azzur
  • 8:30-10:00
    Select Between Knowledge Exchange Sessions (5-8)
  • (5)
    Successful Implementation of a 3-Stage Process Validation Program
    Mehron Mirian, Senior Quality Manager, Molecular Templates
  • (6)
    Risk-Based Cleaning Validation – Key Elements to a Successful Program
    Sunil Patel, Senior Global Technical Leader, Ecolab Life Sciences
  • (7)
    Implementation of a Risk-based Verification Strategy for CQV
    Joscelyn Bowersock, Regulatory and Quality Manager, Carolina BioOncology Institute
  • (8) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Construction of a Data Integrity Program from the Ground Up
    Matthew LaPierre, Data Integrity Program Manager, Ipsen Bioscience
  • 10:00
    Mid-Morning Refreshment Break
  • 10:30-12:00
    Select Between Knowledge Exchange Sessions (9-12)
  • (9)
    Introduction to Validation Statistics for Non-Statisticians
    Raul Soto, Senior Principal Software Engineer, Johnson & Johnson Vision Care
  • (10)
    Key Considerations for Process Validation and Successful Tech Transfer
    Philip Jarvis, Validation Site Lead, Alcon
  • (11)
    Implement a Risk-Based Computer Systems Validation Program
    Lizzandra Rivera, Associate Director, Enterprise – e-Systems, Alexion Pharmaceuticals
  • (12) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Human Performance and Data Integrity - Transforming the Culture
    Danny Hernandez, Associate Director Data Integrity, Bayer
  • 12:00
    Lunch & Learns, Select Between (13-16)
  • (13)
    Training Personnel in Validation Execution
    Chris Wubbolt, Principal Consultant, QACV Consulting, LLC
  • (14)
    Go Beyond Warning Letter Trends and Guidance Documents
    Michael de la Torre, CEO, FDAZilla
  • (15)
    Conduct Risk-Based Revalidations and Periodic Reviews of Systems
    Jorge A. Cordero, Principal Validation Engineer, Bausch + Lomb
  • (16) DATA INTEGRITY INSPECTION READINESS SUMMIT
    CyberSecurity – Protecting Data Against Malicious Threats
    To Be Announced
  • 1:15–2:45
    Select Between Knowledge Exchange Sessions (17-20)
  • (17)
    Risk-based IQ/OQ/PQ Development and Execution
    Jorge A. Cordero, BSChE, MBA-GM, Principal Validation Engineer, Bausch + Lomb
  • (18)
    Medical Device Process Validation Implementation Case Study
    David W. Vincent, Ph.D., CEO, VTI Life Sciences
  • (19)
    Hiring the People Who Make Validation Great
    Patrick Mullin, Senior CQV/QAV Consultant, DPS Group Global
  • (20) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Data Integrity Assessments – Moving Past Assessment to Implementation
    Lizzandra Rivera, Associate Director, Quality – IT, Alexion Pharmaceuticals
  • 2:45
    Afternoon Refreshment Break
  • 3:15– 4:45
    Select Between Knowledge Exchange Sessions (21-24)
  • (21)
    Apply Quality Risk Management (QRM) in Validation Processes
    Connie Hetzler, Global Head of Validation, Alcon Laboratories
  • (22)
    The Validation Master Plan (VMP) – Plans that Impress FDA Investigators
    David W. Vincent, Ph.D., CEO, VTI Life Sciences
  • (23)
    Performance Qualification Versus Process Validation
    Erik Muegge, M.S., Manager Operations Quality, Abbott Laboratories
  • (24) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Data Integrity – Remediation Projects and Building for the Future
    Alice Redmond, Vice President European Operations, Commissioning Agents Inc.
  • 4:45 Day Two Closing Session
    Considerations for Using Spreadsheets in a GxP Compliant Environment
    Sanjay Agrawal, President and CEO, CIMINFO Software
  • Close Of Day Two
  • 7:00
    Coffee and Lite Breakfast
  • 7:30–8:15
    Select Between Knowledge Exchange Breakfasts (25-28)
  • (25)
    CQV Master Class – Benchmark with Your Peers
    Alice Redmond, Vice President European Operations, Commissioning Agents Inc.
  • (26)
    Managing Changes in Validation Processes
    Mehron Mirian, Senior Quality Manager, Molecular Templates
  • (27)
    Prepare for Validation Inspections and Respond to Findings
    Milan Kalinic, Validation Lead, Alexion Pharmaceuticals
  • (28) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Data Integrity Risk Assessments – Using Process Flow Charts
    Chinmoy Roy, Industry Consultant, ValGenesis Inc
  • 8:30–10:00
    Select Between Knowledge Exchange Sessions (29-32)
  • (29)
    Continued Process Verification (CPV) – Maintain the Validation State
    Philip Jarvis, Site Validation Lead, Alcon
  • (30)
    Network Infrastructure and Cloud Qualification
    Lelia Scott, Senior Director Global Quality Systems, Charles River Laboratories
  • (31)
    Machine Learning – Validation and Data Integrity Compliance
    Steve Thompson, Director Computer Quality Assurance, Science 37
  • (32) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Managing FDA DI Inspections and Responding to Inspectional Findings
    Eileen Cortes, Associate Director for QA and Validation, BioMarin
  • 10:00
    Mid-Morning Refreshment Break
  • 10:30 – 12:00
    Select Between Knowledge Exchange Sessions (33-36)
  • (33)
    Apply Quality Risk Management (QRM) in Equipment Qualification
    Patrick Mullin, Senior CQV/QAV Consultant, DPS Group Global
  • (34)
    Developing and Documenting Quality Test Scripts
    Erik Muegge, M.S., Manager Operations Quality, Abbott Laboratories
  • (35)
    Conduct a Part 11 Gap Assessment
    Chris Wubbolt, Principal Consultant, QACV Consulting, LLC
  • (36) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Real World Case Studies in Data Integrity Audits
    Chinmoy Roy, Industry Consultant, ValGenesis Inc
  • 12:00
    Lunch & Learns, Select Between (37-40)
  • (37)
    Quality by Design in Process Validation
    Joscelyn Bowersock, and Quality and Regulatory Manager, Carolina BioOncology Institute
  • (38)
    Importance of the Quality Agreement in Managing Vendors
    Bette Monnot-Chase, Director, CMC & Quality, Asklepion Pharmaceuticals
  • (39)
    Establish Cleaning Residue Limits and Acceptance Criteria
    Ravi Samavedam, General Manager, Azzur Group
  • (40)
    Automated Risk-Based Data Integrity Processes
    Steve Thompson, Director Computer Quality Assurance, Science 37
  • 1:15- 2:30
    Select Between Knowledge Exchange Sessions (41-43)
  • (41)
    Statistical Process Controls – Construct and Analyze Control Charts
    Raul Soto, Senior Principal Software Engineer, Johnson & Johnson Vision Care
  • (42)
    Qualification Strategies for Temperature Mapping & Storage Chambers
    Bette Monnot-Chase, Director, CMC & Quality, Asklepion Pharmaceuticals
  • (43) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Audit Trail Reviews & Data Integrity Compliance
    Robert J. Wherry, MSc, MS, CPIP, Head – R&D Data Systems QA & Compliance, Takeda
  • 2:30
    Afternoon Refreshment Break
  • 3:00- 4:30
    Select Between Knowledge Exchange Sessions (44-46)
  • (44)
    Equipment Qualification – Fit for Intended Use
    Milan Kilanic, Validation Lead, Alexion Pharmaceuticals
  • (45)
    Using Quality System Elements to Maintain Your Process Validated State
    Gamal Amer, Ph.D. Principal, Premier Compliance Services
  • (46) DATA INTEGRITY INSPECTION READINESS SUMMIT
    Using Validation Sampling Plans for Critical Decisions
    Raul Soto, Senior Principal Software Engineer, Johnson & Johnson Vision Care
  • 4:30
    Close of Conference

Faculty

  • Sanjay Agrawal, President and CEO, CIMINFO Software

    Sanjay Agrawal is President and CEO of CIMINFO Software. He has over 25 years of experience in Computer Systems Validation, and Data Integrity Compliance. Early in his career, Sanjay pioneered risk-based validation methodologies for large scale enterprise systems such as ERP by developing a data framework, and identifying the controls necessary for each data category. He has developed facility-wide Master Validation Plans that included systems, people, and processes and managed validation projects for systems at every level ranging from spreadsheets/databases, PLCs and equipment to LIMS, HPLC, SCADA, MES and ERP. Sanjay is also a pioneer in introducing Part 11 compliance technologies for spreadsheets and Access databases to the industry that are in use today at hundreds of FDA-regulated firms worldwide.
  • Gamal Amer, Ph.D. Principal, Premier Compliance Services

    Dr. Amer, a chemical engineer by training, has 40 years-experience in the pharmaceutical and related industries. He has held senior management positions with leading pharmaceutical, consumer products, and engineering consulting companies. His experience includes comprehensive process design in bulk pharmaceutical chemicals manufacturing, biotechnology manufacturing, pharmaceutical solid dosage manufacturing, and containment of potent and radioactive therapeutics. He is also experienced with facility development for therapeutic products operations. Dr. Amer is a recognized expert in GMP compliance and validation.
  • Joscelyn Bowersock, Regulatory and Quality Manager, Carolina BioOncology Institute

    Ms. Joscelyn Bowersock is a Quality and Regulatory Manager with nineteen years of clinical and research experience; including process implementation and validation, risk mitigation protocols, facility commissioning, and master file development. Her experience has allowed her to successfully implement numerous quality systems, navigate IND submissions, FDA inspections and cell therapy program accreditations.
  • Jorge A. Cordero, BSChE, MBA-GM, Principal Validation Engineer, Bausch + Lomb

    Jorge A. Cordero has over nineteen (19) years of experience in the biotechnology, pharmaceutical, medical devices and municipality industries in the technical services and management areas, including validation, engineering specification, and equipment design specification. Currently, Jorge is working with Bausch + Lomb managing the validation and metrology departments.
  • Parsa Famili, President & CEO, Novatek International

  • Connie Hetzler, Global Head of Validation, Alcon Laboratories

    Ms. Hetzler has over 32 years of experience working in regulated consumer products and healthcare industry roles. In her current role as Global Head of Validation for Alcon, she is accountable for the validation strategy for 16 manufacturing sites including both the surgical and vision care divisions.
  • Philip Jarvis, Site Validation Lead, Alcon

    Phil is an experienced team leader with over ten years of experience in all areas of validation including; process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation. Through strategic thinking, he has success in steering and managing complex validation projects within the medical device and pharmaceutical industries.
  • Milan Kilanic, Validation Lead, Alexion Pharmaceuticals

    Milan Kalinic is Pharmaceutical professional specializing in Sterile Fill Finish and Solid Dosage manufacturing environment with more than 13 years of experience. Currently works as a Validation Lead at Alexion Pharmaceuticals. Previous position includes Validation Specialist at Hemofarm (Member of STADA Arzneimittel Group). Milan was responsible for Leading of cross functional CQV Teams and manufacturing equipment projects delivery within the Hemofarm Group such as: Start-up of the Syringes & Cartridges Manufacturing Site, Start-up of the Ampoules Manufacturing Site and Start-up of the Sterile Nasal Spray Manufacturing Site. Also, he was responsible for leading a Packaging Lines CQV team for start-up of Packaging Center for Solid Dosages Forms. Milan is manufacturing specialist for Filling Lines (CIP/SIP and Isolators), Compounding Systems, Autoclaves, Freeze Dryers, HVAC, Water Systems and Systems for Pharmaceutical Gases.
  • Mehron Mirian, Senior Quality Manager, Molecular Templates

    Mehron Mirian has more than 18 years of experience in Quality and Engineering in the Medical Device, Pharmaceuticals, Biotechnology and Diagnostics industries. Mehron, who holds a BS in Biology, has worked for companies such as Cardinal Health, Bio-Rad, B.Braun, Avid, and Molecular Templates. Mehorn currently manages quality department in Molecular Templates as the Senior Quality Manager.
  • Bette Monnot-Chase, Director, CMC & Quality, Asklepion Pharmaceuticals

    Bette has a strong background in drug development in the areas of analytical method development, stability, formulation, validation, and vendor management. Her main responsibilities included stability, product development and associated analytical testing, as well as preparation of regulatory CMC documents for global filings. Working for small Pharma that adopted a virtual model - outsourcing all CMC activities to third party vendors, Bette has extensive experience managing the need of her projects and the vendor’s needs, which is necessary to delivery high quality analytical methods, robust formulation and critical stability data to support the product in a global clinical or commercial marketplace.
  • Erik Muegge, M.S., Manager Operations Quality, Abbott Laboratories

    Erik Muegge’s experience is focused on FDA and related regulated environments for pharmaceuticals, consumer products, and medical devices. His specific areas of work include Quality Systems, operations, outsourcing, process re-engineering, project management, product development life cycle (R&D through Launch) and validation. Erik has; led efforts in several PPC (Production and Process Controls) areas; harmonized validation activities globally across seven sites; audited quality systems of strategic partners; been recognized as a global SME resulting in three industry awards.
  • Patrick Mullin, Senior CQV/QAV Consultant, DPS Group Global

    Patrick Mullin has over 15 years of experience in vaccine and biotech operations which include commissioning, qualification, and validation (CQV) management for clinical and commercial scale biotech operations. Patrick's core focus is with the creation, implementation, and maintenance of CQV programs specializing in critical utilities, process equipment (upstream/downstream production and fill finish), process automated systems, and sterilization/cleaning support systems at pilot plant and full commercial scales.
  • Lizzandra Rivera, Associate Director, Quality – IT, Alexion Pharmaceuticals

    Mrs. Rivera is a pharmaceutical professional with over 15 years of experience in validation and quality compliance. A Chemical Engineer graduate from the University of Puerto Rico, she has provided strategic leadership and tactical implementation guidance to establish a wide range of computerized systems and equipment, ensuring regulatory compliance is maintained throughout the systems’ lifecycles. She has a well-rounded background encompassing manufacturing, IT and quality assurance.
  • Ravi Samavedam, General Manager, Azzur Group

  • Lelia Scott, Sr. Director Global Quality Systems, Charles River Laboratories

    Ms. Scott is a senior management quality professional with 14 years of progressively challenging QA experience within the pharmaceutical industry, and 7 years’ in analytical lab sciences. Her specializations include: global process adoption, implementation of enterprise-wide quality systems, global computer system validation, laboratory systems, relationship building in cross-functional teams and development of innovative solutions to expedite business processes using electronic systems in compliance with global pharmaceutical regulations. She holds a Bachelor in Chemistry from the University of Western Ontario and an MBA in Pharmaceutical Management from Fairleigh Dickinson University
  • Raul Soto, Senior Principal Software Engineer, Johnson & Johnson Vision Care

  • David W. Vincent, Ph.D., CEO, VTI Life Sciences

    Mr. Vincent has over 33 years’ experience in the health care industry specializing in the, biologic, biotechnology and biopharmaceutical industries and has over 25 years dedicated to the field of validation. Mr. Vincent has provided both project management and project execution for numerous clients national and international. He is responsible for managing and supporting many different product launches. He teaches at San Diego State University (SDSU) for their Masters of Regulatory Affairs Degree program in the Field of Validation Technology RA-776.
  • Robert J. Wherry, MSc, MS, CQA, CPGP, CPIP, Head – R&D Data Systems QA & Compliance, Takeda

    Mr. Wherry has thirty-five (35) years of international pharmaceutical, biotechnology and medical device experience with expertise in Computerized System Validation, Data Integrity, Quality Systems, Process Validation, Aseptic Processing, Regulatory Operations and eCTD submissions. He has served as an industry consultant, performing data integrity audits around the globe at multiple companies. Bob currently is the Head of R&D Data Systems Quality Assurance and Compliance for Takeda, in Lexington, Massachusetts, and teaches part-time as an Adjunct Professor within the STEM Division's Biotechnology Program at Middlesex Community College in Massachusetts. Mr. Wherry has a Bachelor’s degree in Chemical Engineering from Lehigh University. He has a Master of Science, with distinction, from the University of Strathclyde (Glascow, UK) in Pharmaceutical Quality & GMP. He also has a Master of Science in Regulatory Affairs from Northeastern University. Bob also has certifications from ASQ and ISPE.
  • Chris Wubbolt, Principal Consultant, QACV Consulting, LLC

    Chris Wubbolt is a Certified Six Sigma Black Belt, has a Masters Degree in Quality Assurance and Regulatory Affairs and a BS in Physics and Computer Engineering. Mr. Wubbolt was the previous President of both the New England Region Chapter Society of Quality Assurance (NERCSQA) and the Mid-Atlantic Region Society of Quality Assurance (MARSQA), and is currently the chairperson of the MARSQA computer validation committee.

Sponsors

  • GOLD




  • A nationwide network of experts delivering professional services across the life sciences industry, Azzur Group is dedicated to providing clients with efficient, innovative quality and compliance solutions from Discovery to Delivery™. With more than 250 industry partners, including 80% of the top pharma/biotech manufacturers in the U.S., Azzur Group provides carefully calibrated and efficiently executed project management, process engineering, and compliance services. As one of the fastest growing private companies in America, Azzur Group provides clients with the consulting, facility solutions, engineering, validation, IT, technical, training, and laboratory services and solutions they need to remain innovative and competitive.
    Website: https://www.azzur.com/
  • Since 1949, Ellab is a leading manufacturer of a full line of wireless, real-time data loggers and wired thermocouple validation systems with temperature, humidity, pressure, vacuum, conductivity and CO2 sensor options. Additionally, Ellab offers temperature standards, calibration dry blocks and liquid baths, custom fittings, accessories, and thermocouples. We also offer on-site qualification, validation and calibration services for thermal validation processes ranging from -196°C to 400°C. Typical environments often include -80°C freezers, incubators, stability chambers, autoclaves, and ovens.

    Website: https://www.ellab.com/
  • For almost sixty years, Kaye has been at the forefront of high accuracy process measurement. For applications from thermal process validation and environmental monitoring, to sensor calibration, Kaye technology has provided the most accurate and user friendly measuring systems available in the market today.

    Kaye equipment has become the standard for helping customers increase validation process efficiency and document the results. The Kaye product range is designed to meet the most demanding industrial requirements for process improvement, thermal validation and reporting. Specializing in providing turnkey system solutions and supporting them with unmatched technical service, we offer a complete range of wired systems, wireless systems, RF-based real-time systems, temperature standards, baths, thermocouples and fittings, all designed to provide the most accurate process measurement available.
    Website: https://www.kayeinstruments.com
  • SILVER




  • Trusted by hundreds of FDA-regulated firms in over 30 countries, CIMINFO provides Data Integrity and 21 CFR Part 11 compliance solutions that reduce compliance costs and improve efficiency. Existing spreadsheets and Access databases can be made Part 11 compliant with minimal effort. Enterprise products automate business processes such as data integrity management/auditing, document management, engineering data/drawing controls, and training.
    Website: https://part11solutions.com/
  • Ecolab is the global leader in water, hygiene and energy technologies and services. Every day, we help make the world cleaner, safer and healthier – protecting people and vital resources.
    Website: https://www.ecolab.com/
  • FDAzilla, a subsidiary of Govzilla, is at the forefront of leveraging the power of Big Data and AI to make government data accessible, usable and valuable to everyone who needs it. Top Pharma Companies, Food Manufacturers, Medical Device Companies, and Service firms from around the globe rely on Govzilla to mine and process government inspection, enforcement, and registration data in order to quantify risk signals about their suppliers, identify market opportunities, benchmark against their peers, and to prepare for the latest inspection trends. Our data and analytics have been cited by major media outlets such as MSNBC, WSJ, and the Boston Globe. Our website, FDAzilla.com is viewed more than 1 million times per year. We are passionate about our mission to solve novel data and analytics problems for our customers. At Govzilla, we’re committed to our work, to our customers, and to having fun.
    Website: https://fdazilla.com/
  • Novatek International’s mission is to produce regulatory compliant software solutions to the pharmaceutical, biotech and other health-care industries. Our goal is to improve patient safety by producing solutions that reduce the risks associated with pharmaceutical manufacturing and contribute to product quality.
    Website: https://ntint.com/
  • QACV offers comprehensive quality assurance, compliance, and computer validation consulting services to meet your regulatory needs. We provide professional consulting services to FDA regulated life science industries and use proven methodologies to achieve sustainable compliance for your organization.
    Website: http://www.qacvconsulting.com/
  • We have expertise in the practical implementation of a wide range of statistical methodologies in all parts of the pharmaceutical product lifecycle.
    Website: https://www.synolostats.com/
  • Global Leader in Paperless Validation
    Website: http://www.valgenesis.com
  • Inspiring Operational Excellence through Best-in-Class CQV Processes
    Website: http://www.validation.org

Partners

Venue

Details

Start:
March 25
End:
March 27
Event Category:

Venue

Wyndham Philadelphia Historic District
400 Arch Street
Philadelphia, PA 19106 United States
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Phone:
(215) 923-8660
Website:
https://book.passkey.com/event/49826319/owner/16417/home

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