PD 6630:1998, CR 13217:1998 - Comprehensive Guide to Health Care Technology Standards

The PD 6630:1998, CR 13217:1998 document is an essential resource for healthcare technology professionals, ensuring the highest standards of safety, effectiveness, and quality in medical device performance. Published on September 15, 1998, this standard serves as a critical reference for manufacturers, assessors, and regulatory bodies engaged in health care technology.

Purpose and Scope

This document delineates the necessary frameworks and criteria for evaluating various types of health care technology. It comprehensively addresses essential requirements such as technical specifications, performance benchmarks, and user safety protocols. By adhering to the guidelines established in PD 6630:1998, stakeholders can assuredly navigate the intricacies of health technology deployment.

Key Features

• Identical Versatility: The CR 13217:1998 classification aligns perfectly with PD 6630:1998, providing consistency and reliable reference points in healthcare technology standards.
• Comprehensive Documentation: This standard includes detailed descriptions of testing procedures, assessment methodologies, and risk management strategies that supplement the overarching framework.
• Universal Applicability: Whether you are developing new medical devices or evaluating existing technologies, this document equips you with the necessary tools to maintain compliance and uphold safety protocols.

Importance of Standards

In today's rapidly evolving health care landscape, the adherence to recognized standards like PD 6630:1998 is paramount. Ensuring compliance helps mitigate risks associated with medical technology utilization while advancing patient outcomes and satisfaction. Standards facilitate clear communication among professionals and foster innovation through a unified approach to safety and efficacy.

Who Should Use This Document?

The PD 6630:1998, CR 13217:1998 document is indispensable for a variety of professionals including:

• Medical device manufacturers seeking to uphold quality and compliance.
• Healthcare professionals who require a steadfast understanding of technology capabilities.
• Regulatory bodies responsible for assessing and granting approvals for medical technologies.
• Academic institutions and research organizations engaged in health technology studies.

Purchase Information

The PD 6630:1998, CR 13217:1998 document is available in both PDF and hardcopy formats, ensuring accessibility for all users. With an investment of £158.00, you can procure this vital resource and align your practices with the latest health care technology standards.

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