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Medical Eclipse Af Study Services In Usa
5 services found
by:Harris Healthcare based inNiagara Falls, NEW YORK (USA)
While we would not self-classify as having a clinical research management system (i.e. research-specific grant application preparation, funding management, and cost accounting features are not available), clients effectively use our solutions for clinical research projects. We provide the flexibility needed to capture, access and control data quality while complying with regulations and industry ...
by:Integra IT based inBogotá, COLORADO (USA)
Thanks to our engineers and clinical research professionals, we can streamline clinical trials startup times, enrich data and accelerate submissions. Through advanced methodologies and high skill professionals from Latin America, our services empowered by technology accelerate deliverables with quality and compliance over a very cost-convenient ...
by:in2being, LLC based inSaline, MICHIGAN (USA)
The Food and Drug Administration (FDA) regulates all medical devices in the United States to make sure they are safe and effective. These regulations are a critical part of the medical device development process, and they will likely influence the design and testing of new medical devices. Navigating the medical device regulation process is complicated, and if you don’t correctly adhere to ...
Manufactured by:Ceutical Labs based inFlower Mound, TEXAS (USA)
There are several distinct markets that are served by the Analytical Testing Division. They include Pharmaceutical, Nutraceutical, Medical Device, API (Active Pharmaceutical Ingredient), NDI (New Dietary Ingredient) and Post Sterilization Testing. Two of these categories, API and NDI require additional explanation. Their definitions are as follows: API -An API is an active pharmaceutical ...
Manufactured by:KSL Biomedical based inBuffalo, NEW YORK (USA)
KSL Biomedical, Inc. (“KSL”) was founded to deliver innovative diagnostics and therapeutics. KSL has professionals with many decades of experience in US and international regulatory compliance, product design and development, clinical trials, and protection of intellectual property to work with health care industry partners to address their need for special resources to achieve and ...