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Surpass Inc.
11 followers -
Trusted preclinical contract research organization (CRO) partner for medical device, pharmaceutical and biotech companies
Trusted preclinical contract research organization (CRO) partner for medical device, pharmaceutical and biotech companies

11 followers
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Happy holidays from your friends and preclinical research partners at Surpass

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Attending the MN Medtech Week Nov 4-5?

Stop by our booth (2139) and play Medical Translation with us! We'll have games highlighting appropriate models for different types of medical devices and will be handing out free copies of our WHITE PAPERS and the MEDTECH STRATEGIST by David Cassak and Stephen Levin, co-founders of Innovation In Medtech.

Contact Surpass for free expo passes for the event 715.294.4371 or 650.938.3675.
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Are you planning a bioskills training or R&D cadaver study for your medical device? Check out Surpass' latest post on how to select the best preclinical research facility.

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Surpass CEO, Dr. Tim Pelura, will be presenting "Value-Driven Innovation -Tactical Considerations for Preclinical Study Design" at the upcoming Emerging Medical Technologies Summit, October 19-21st in Redwood City, CA. If you are attending the event, stop by our table to learn how Surpass can help you translate your medical concepts into reality through preclinical research.

http://www.lifescienceintelligence.com/emerging-medical-technology-conference-agenda3.php
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Yesterday FDA issued a new draft guidance related to preclinical studies, GENERAL CONSIDERATIONS FOR ANIMAL STUDIES FOR MEDICAL DEVICES. Be sure to check it out and provide them your feedback before it is finalized. As always, the Surpass team stands ready to assist with the preclinical studies component of your submission package.

http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/UCM466358.pdf?source=govdelivery&utm_medium=email&utm_source=govdelivery
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Surpass will be at TCT this week in San Francisco (booth 2340). Don't miss this opportunity to meet with our team to discuss your upcoming projects. We've helped hundreds of companies translate their medical product concepts into reality through preclinical research. We can do the same for you.
http://www.crf.org/tct

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Surpass is pleased to announce we had a successful FDA GLP surveillance inspection at our Silicon Valley facility this past week and no 483 was issued. We're proud of the Surpass team!
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Are you planning a medical device GLP study in the near future?
Be sure your test articles are labeled appropriately to help prevent mix ups. Check out our blog post describing considerations for test article labeling. bit.ly/GLPhints_article2
Contact us to learn more about Surpass' GLP services.
Silicon Valley: 650.938.3675 or Greater Twin Cities: 715.294.4371
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Are you developing a Cardiovascular Device or Therapy? Surpass has proven experience helping clients translate their medical products into reality. Learn more! http://www.surpassinc.com/expertise/cardiac/
http://www.surpassinc.com/expertise/vascular/
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