Visionary Standards: Advancing Sci & Reg in Generic Ophthalmic Products
Gain insights into the intricacies of developing ophthalmic products, including insertable, implantable, & topical ophthalmic therapies
Date and time
Location
The Universities at Shady Grove
9630 Gudelsky Drive Rockville, MD 20850Agenda
8:50 AM - 11:40 AM
D1 S1: Ophthalmic Product Standards and General BE Considerations
12:40 PM - 3:00 PM
D1 S2: Regulatory Science Applied to Ophthalmic Dispersion Products
4:00 PM - 5:30 PM
D1 S3: Session 3: Small-Group Sessions (In-person only)
9:10 AM - 11:40 AM
D2 S4: Regulatory Sci Applied to Ophthalmic Insertable & Implantable Products
1:00 PM - 3:05 PM
D2 S5: Regulatory Science Applied to Drug-Device Combination Products
3:20 PM - 5:00 PM
D2 S6: Small-Group Discussion Tables (In-person only)
Good to know
Highlights
- 1 day 8 hours
- In person
- Paid parking
- Doors at 7:45 AM
Refund Policy
About this event
The field of generic ophthalmic drug products is rapidly evolving, with increasing complexity in drug product formulations and devices, leading to challenges in assessing performance sameness and ensuring quality. In response to these evolving complexities, this workshop is designed to address the latest advancements and regulatory challenges in the field, offering a unique platform to engage with all relevant parties, share knowledge, and contribute to the evolution of generic development and regulatory assessment.
Attendees will gain valuable insights into the intricacies of developing ophthalmic products, including insertable, implantable, and topical ophthalmic therapies. In addition to a series of expert-led presentations and panel discussions, in-person attendees will interact directly with regulators, industrial peers, and academic experts in small group working sessions to deepen their understanding of current practices and challenges, regulatory expectations, and emerging trends.
Specifically, the two-day workshop will cover critical issues such as in vitro drug release testing, qualitative (Q1) and quantitative (Q2) sameness of complex ingredients in ophthalmic products, formulation characterization, considerations for clinical bioequivalence studies, and the challenges encountered when developing or assessing prospective generic ophthalmic products.
Registration Fees:
- This workshop is FREE for virtual attendees.
- The combined cost for the two-day workshop in-person attendance and activities is:
- $350, in-person attendees - general
- $150, in-person attendees - government (must have an email ending in ".gov" to register at this rate)
For in-person attendees, beverages and food for breaks will be provided; lunch is not included. A link will be provided closer to the event for ordering lunch each day.
For faculty and students from the University of Maryland, Baltimore; The Universities at Shady Grove; and University of Michigan, the workshop is free for in-person attendance. Other students, please email CRCG for a reduced rate. Contact CRCG at (info@complexgenerics.org) and indicate which workshop you are interested in.
Continuing education (CE) credits will not be provided for attending this workshop. A certificate of attendance will only be provided to individuals attending the workshop in-person, when requested.
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