< 1 min reading time Looking for recommendations on Clinical Research Organisations to undertake phase 1/2 clinical trials for a newly developed medical device and a therapy. source: https://www.linkedin.com/groups/78665/78665-6380263623817719811 Marked as spam |
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Private answer Talk with Anne Leijsen from Factory CRO. She's speaking at the 10x Medical Device Conference in two weeks. Marked as spam | |
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Private answer Talk to me if you’re keen to explore Australia or New Zealand. So many great reasons why. Drop me an email [email protected] Marked as spam | |
Private answer Julie Omohundro Trials to be conducted in Australia? To support CE Marking? Marked as spam | |
Private answer Julie Omohundro PS When someone has never worked in the device industry or been involved in clinical trials is the person who is looking for a device CRO, that's usually not a good sign. Marked as spam | |
Private answer Talk to me if you are keen to explore india. Drop me an e.mail: [email protected] Marked as spam | |
Private answer Dennis King Always happy to talk with you about clinical trial services for US Regulatory Approval Studies. www.statkingclinical.com Marked as spam | |
Private answer Iván Parra Guerra Good morning, we would be happy to help you. In ZURKO RESEARCH We are d in clinical trials in Medical Devices Marked as spam | |
Private answer Iván Parra Guerra Good morning Dr. Andrew, we would be happy to help you. In ZURKO RESEARCH We are specialists in clinical trials in Medical Devices, with rapid response and protocol designs Marked as spam | |
Private answer Dr. Dieter Werdier For trials inside the EU contact us. SAM GmbH, Aachen, Germany Marked as spam | |
Private answer Beluh Mabasa Ginting The question is whether all CRO must comply to the ISO 14155:2011, Clinical investigation of medical devices for human subjects - Good clinical practice..? Marked as spam | |
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