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2025 RAC Workshop
Virtual Event - Webinar Only
Durham, NC 27701
USA
Tuesday, June 03, 2025, 6:00 PM - 8:00 PM EDT
Category: RAC Workshop

 This workshop will have live sessions every Tuesday evening, 6 -8 pm, starting June 3, 2025 and running through September 30, 2025; see the confirmation email for all session dates. 

The sessions will be REMOTE; held via Zoom.


REGISTER HERE

The Zoom meeting info can be found in the confirmation email received after you register.

 

 

PHARM/BIO

 

 

 

 

2025 Chapter

Speaker

Topic

 

 

June 3

1

1 - Intro

Maria Oyaski

FDA History (create study groups)

June 10

2

1 - Intro

Kevin Barber

Regulatory Authority Meetings

June 17

3

1 - Intro

Olu Aloba

CMC (drugs and biologics)

June 24

4

2 - Early development

Brenda Faiola

Preclinical Development and GLPs

July 1

No presentation; July 4th week.

July 8

5

2 - Early development

Matthew Barnes

Clinical Protocols and Clinical Development Plans

July 15

6

2 - Early development

David Jensen

Good Clinical Practice

July 22

7

2 - Early development

Judy Hauser

Combination Products

July 29

8

3 - Regulatory Procedures

Karl Whitney

INDs, IMPDs, CTAs, & CTXs

Aug. 5

9

3 - Regulatory Procedures

Sheila Plant

NDAs/BLAs, MAAs, JNDAs, NDSs

Aug. 12

10

3 - Regulatory Procedures

Erin O’Reilly

Pediatric, Orphan Product and Expanded Access Development for Rare Diseases

Aug. 19

11

4 -Specific product types

Catherine Maher

Pharmaceuticals, Generics, and OTC Drugs

Aug. 26

12

4 -Specific product types

Maria Oyaski

Biologics and Biosimilars

Sep. 2

13

4 -Specific product types

Maria Oyaski

Advanced Medicinal Therapeutic Products

Sep. 9

14

5 – Late development

TBD

Pharmacovigilance and Risk Management

Sep. 16

15

5 – Late development

TBD

Prescription Product Labeling

Sep 23

16

5 – Late development

Drew Barlow

Compliance, Regulatory Inspections, and Enforcement

Sep 30

17

5 – Late development

Patricia Termini

Post Marketing

 

 

 


Contact: [email protected]