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Emergo by UL is a leading consulting firm specializing in global regulatory compliance and human factors for products in the medical industry. Our comprehensive services are designed to help you achieve and maintain regulatory and commercial success.
Emergo was founded in 1997 with a mission to help medical device and IVD manufacturers manage regulatory affairs compliance and expand into new markets. We have grown into a global solutions provider specializing in end-to-end regulatory affairs/quality assurance life cycle management.
Emergo by UL user research and human factors specialists share tips for using ethnographic research to augment human factors activities throughout medical device development. Page 1 of 39. Get the latest global medical device regulatory news, insights from our experts and more.
Emergo by UL | 15,298 followers on LinkedIn. Emergo provides quality and regulatory compliance consulting to medical device and IVD companies.
我们专业从事全球医疗器械和体外诊断器械的合规和创新服务。Emergo帮助人们获得更安全、更可靠的服务、 体验和环境——做出明智的选择，享受更好的生活。
Simplify EU medical device regulatory compliance. Developed by experts at Emergo by UL, RAMS offers a growing portfolio of EU MDD, MDR and IVDR services, including Product Classification and seven Smart Builders, that deliver critical assistance to companies transitioning to Europe’s new regulatory scheme. Try now.
Emergo provides quality and regulatory compliance consulting to medical device and IVD companies. We assist with medical device registration/approval, regulatory strategy, ISO 13485 and QMS...
