Home Medical Device Retail Exemptee Online Training Certificate – HMDR

The Home Medical Device Retailer Exemptee License Application requires proof of HMDR Exemptee training program completion.

SkillsPlus International Inc. offers an Exemptee training program (that covers topics specified by the California Dept of Public Health – Food and Drug Branch). Upon successful completion of this training course, the student will receive a certificate of completion, that is acceptable to the CDPH FDB.

Learn more about Exemptee training by SkillsPlus Intl Inc.
Buy and register now! – SkillsPlus Intl Inc. Exemptee Training Course

HMDR Exemptee Training

 


Go to DREprof.com: The Designated Representative and Exemptee Training Website

Wholesaler Application Instructions – CA Board of Pharmacy

Drug capsules orbiting the earth

“A wholesaler permit is required before any firm or organization who sells for resale or negotiates for distribution, may distribute, broker or transact the sale or return of dangerous drugs or dangerous devices in California. Wholesalers sell and distribute dangerous drugs and dangerous devices (also called “legend” items or prescription-required drugs and devices) to other business entities who are authorized by law to purchase the items or sell to licensed health care providers who are authorized by law to possess the dangerous drugs and dangerous devices.”

View the complete set of instructions: Source: California Board of Pharmacy – Wholesaler Application Instructions

Drug wholesaler applicants will also need to have a Designated Representative.
SkillsPlus Intl Inc. offers an online training course designed for Designated Representative applicants.


Go to DREprof.com: The Designated Representative and Exemptee Training Website

Refurbished Medical Devices: FDA Wants to Hear More From Industry | RAPS

FDA logo

“The US Food and Drug Administration (FDA) on Thursday announced that it’s seeking more information on medical devices that are refurbished, reconditioned, rebuilt, remarketed, remanufactured, serviced or repaired in order to investigate a number of potential safety issues.”

Read the full article:  Source: Refurbished Medical Devices: FDA Wants to Hear More From Industry | RAPS

Read the proposed rule:
Refurbishing, Reconditioning, Rebuilding, Remarketing, Remanufacturing, and Servicing of Medical Devices Performed by Third-Party Entities and Original Equipment Manufacturers; Request for Comments


Go to DREprof.com: The Designated Representative and Exemptee Training Website

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