Gerald96
02-19-2007, 08:50 PM
The roles of regulatory healthcare professionals are defined by their obligations as employees of companies that make important medical products and services for patients, as members of teams that conduct non-clinical and clinical studies and as regulators in the Regulatory World (http://www.regulatoryworld.com/php/index.php) of healthcare.
These healthcare professionals in the Regulatory World (http://www.regulatoryworld.com/php/index.php) of medicine have a primary duty to the unbiased dissemination and interpretation of relevant governmental regulations, industry standards and good practice guidelines. They have a duty to ensure products are safe and beneficial to the patents while maintaining the long-term interests of the employers. The regulatory professionals also have a commitment to those who participate in clinical studies and who use regulated products to ensure that, to the extent possible, the benefits justify the risks.
The professionals in the Regulatory World (http://www.regulatoryworld.com/php/index.php) of healthcare also have a duty to provide physicians and other healthcare professionals with complete and accurate information about the safety and effectiveness of the products. They also have to strive to maintain the long-time integrity of the profession. The regulatory affairs professionals are expected to exhibit the knowledge, abilities and skills necessary to effectively identify, analyze and solve or recommend solutions to regulatory challenges. The diversity of individuals and organizational contexts within the professions in the Regulatory World (http://www.regulatoryworld.com/php/index.php) necessitates commitment to a standard level of knowledge. This standard may be achieved through a variety of means: education, work experience, and professional training and certifications.
These healthcare professionals in the Regulatory World (http://www.regulatoryworld.com/php/index.php) of medicine have a primary duty to the unbiased dissemination and interpretation of relevant governmental regulations, industry standards and good practice guidelines. They have a duty to ensure products are safe and beneficial to the patents while maintaining the long-term interests of the employers. The regulatory professionals also have a commitment to those who participate in clinical studies and who use regulated products to ensure that, to the extent possible, the benefits justify the risks.
The professionals in the Regulatory World (http://www.regulatoryworld.com/php/index.php) of healthcare also have a duty to provide physicians and other healthcare professionals with complete and accurate information about the safety and effectiveness of the products. They also have to strive to maintain the long-time integrity of the profession. The regulatory affairs professionals are expected to exhibit the knowledge, abilities and skills necessary to effectively identify, analyze and solve or recommend solutions to regulatory challenges. The diversity of individuals and organizational contexts within the professions in the Regulatory World (http://www.regulatoryworld.com/php/index.php) necessitates commitment to a standard level of knowledge. This standard may be achieved through a variety of means: education, work experience, and professional training and certifications.