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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
Sep 8, 2025 — Sep 10, 2025
  • Conference

Parenteral Drug Association (PDA) Regulatory Conference 2025

Connect with ULTRUS™ ComplianceWire® to explore our qualification platform for compliance, suppliers, clinical and medical education.

people shaking hands at event

Date & Time

Starts

Sep 8, 2025 8:30am EDT

Ends

Sep 10, 2025 6:00pm EDT

Location

Washington, D.C., United States

Language

English

Are you ready to redefine your approach to regulatory compliance and qualification? Join ULTRUS™ ComplianceWire® experts at the PDA Regulatory Conference 2025, where we’ll be showcasing the latest innovations in our platform — designed to meet the evolving needs of life sciences organizations.

This year, we’re spotlighting two transformative solutions:

  • ULTRUS™ ComplianceWire® Clinical Qualification – Streamline and automate the qualification and compliance process across global sites to support consistency and audit-readiness.
  • ULTRUS™ ComplianceWire® Supplier Qualification – Helps highly regulated businesses elevate and maintain supplier compliance to meet regulatory and industry standards.

At ComplianceWire®, we’re committed to helping pharmaceutical, biologics and medical device companies stay ahead of regulatory demands.

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