Partnering with Celegence will see the joint organization’s total number of employees increase to 150, with the addition of two offices in the Netherlands and Romania. Celegence currently has offices in Chicago, London and Bangalore.
Celegence helps life sciences companies navigate complex global regulatory requirements by providing consulting services and solutions dedicated to regulatory affairs. Celegence supports life science customers in the areas of EU MDR compliance, IVDR compliance, regulatory intelligence, RIMS data management, publishing, regulatory labeling including UDI consulting, and medical writing. Celegence’s depth of experience and extensive delivery capabilities allow regulatory affairs and quality teams to operate more efficiently, reduce cost, and improve compliance. For more information, contact us online or follow us on LinkedIn.
Qdossier helps life sciences organizations record and exchange proof of quality, safety and efficacy of medicinal products. Its team of experts boast a wealth of experience in regulatory affairs and electronic submissions, specializing in right first time eCTD lifecycle management and regulatory information management. Supported by Dossplorer™, Qdossier’s advanced cloud-based dossier management solution, the firm’s areas of expertise include regulatory information management, lean and structured authoring, IDMP, and regulatory strategy and procedural support. For more information, visit www.qdossier.com.