Press Release

MD&M West 2017: StarFish exhibits, Christine Park presents Unleashing The Impact of Color

January 3, 2017


VICTORIA, British Columbia, January 3, 2017 – StarFish Medical will exhibit in booth 450 at MD&M West Expo on February 7-9, 2017 at the Anaheim Convention Center, Anaheim, CA.  Charles Garcia, StarFish Medical VP Business Development will be showing a range of medical devices. Use promo code “INVITE” to receive FREE admission to the expo or 20% off of the conference. More information.

CEO Scott Phillips will chair the User-Centric Design track on February 7, and present the opening remarks at 8:25 am.


Christine Park

Starfish Medical Industrial Designer, Christine Park, will present Unleashing The Impact of Color in Medical Device Design to Improve Patient Adoption and Use on February 7, as part of the Medical: Design conference track.  Her presentation will include:

  • Using color to communicate emotion and put patients at ease
  • What types of emotional effects/responses can you get from users?
  • How to make a product more approachable

MD&M West expo is the largest collection of advanced design and manufacturing technology suppliers in the world. Over three days, more than 20,000 professionals source products and services for the development of life-saving medical innovations in a time-saving format with more than 2,200 solution providers—all in one location.

About StarFish Medical:
StarFish Medical provides award-winning design, development, and flexible manufacturing outsourcing services —100% dedicated to the medical device and life science marketplace. StarFish partners with innovative companies to create and manufacture breakthrough products for a full range of medical specialty areas including: Cardiovascular, Digital Health, IVD, Ophthalmology, Optics, and Ultrasound. StarFish expertise includes electronics, mechanical, human factors and software systems engineering.

Our proprietary Pathfinder™ process for medical device product definition saves clients time and resources throughout the technology and product development phases to commercialization. Prototype and low volume complex electro-mechanical production are delivered in an ISO 13485 certified facility with FDA registration, including cleanroom capabilities.

Regulatory and quality system (QMS) consultants at StarFish provide technical regulatory assistance for FDA and Health Canada submissions, including IEC 60601 and ISO13485.

StarFish Medical Media Contact: Mike Camplin | | 250.388.3531 ext. 210 |

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