At Anzil, we maintain procedural standards for every business function of the company. Our comprehensive evaluation and monitoring system ensures effective and timely deliveries
Anzil team includes a pool of highly qualified and diverse professionals with an optimum mix of experience and enthusiasm. Along with our in-house engineering team, we have a comprehensive network of external specialist consultants and partners whose knowledge can be accessed for a total comprehensive solution. Our team has diverse experience in various industries and are well equipped to work on international client projects.
The company is well-positioned to offer customers the established benefits of offshore outsourcing.
Medical Product Design in the Medical Device Life-Cycle is a crucial phase to ensure the safety and efficacy of the product.
Anzil Meditech can support you to train and write verifiable, clear, and concise, traceable requirements, and conduct requirements management at the system level, subsystem level, and component level by understanding your medical device thoroughly. For this, Anzil has an experienced team in the medical device industry.
Anzil follows the standard requirement-based approach to prepare the Design History File (DHF), which ensures the completeness of documents. Our team has extensive experience in developing the Design Document as per US FDA 21 CFR 820.30 and ISO 13485:2016 for all classes of the Medical device.