Pamela Wible MD

MAY 21, 2025

Contact Dr. Wible to save your spot for the ultimate Oregon coast physician retreat—and become the author your patients are searching for. Join our private physician entrepreneur retreat where you’ll receive 1:1 guidance to build a coaching or consulting practice that reflects your passions and expertise. Ready to be your own boss?

Private Practice 180

Private Practice Consulting Medical Student Engineering 180

FDA Law Blog

SEPTEMBER 20, 2021

From new initiatives to facilitate faster reviews for new indications under the Split Real Time Application Review (STAR) pilot program, to bringing new meetings under PDUFA goals, to continued support for rare diseases and incorporation of the patient voice, the goals letter revealed a good number of welcome announcements.

Patient-Centered 52

Patient-Centered Manufacturing Clinic Provider 52

FDA Law Blog

JULY 7, 2024

The guidance restates the central premise of the final rule, i.e., that LDTs are medical devices and the clinical laboratories that design, manufacture and use them to test patient specimens are manufacturers. report certain device malfunctions, and. establish and maintain adverse event files.” [9]

Manufacturing 64

Manufacturing Provider Physicals Electronics 64

Physician's Weekly

JUNE 26, 2025

Gavin Newsom has asked lawmakers to push the implementation date to January 2026, leaving patients, insurers, and employers in limbo. During IVF, a patient’s eggs are retrieved, combined with sperm in a lab, and then transferred to a person’s uterus. A single cycle can total around $25,000 , out of reach for many.

Insurance 52

Insurance Patient-Centered Provider Management 52