Press release
Latest version of IndexFDA adds cross-indexed, searchable 21 US Code content
"The new release allows users to quickly find FDA Warning Letters while searching through the USC," said Michael J. Gregor of ComplianceDoc, Inc. "IndexFDA associates FDA Warning Letters through a cross-index of information to a specific section of Title 21 USC. Our customers rave about our product's ability to seamlessly find information."
Gregor states, "The IndexFDA product is revolutionizing the way industry locates FDA information. Corporations in the Cosmetic, Drug, Food, Legal, and Medical Device industries constantly struggle to find the information they need to determine FDA and industry trends, analyze and assess FDA compliance within their respective organization, and make informed decisions. In essence, the IndexFDA product provides a catalyst for the industry to ensure the highest level of consumer safety and efficacy."
IndexFDA.com provides a powerful, yet well organized and categorized, FDA Regulation, USC, and Warning Letter search database with almost 8,500 FDA Warning Letters to date. Consulting services include Auditing, Computer System Validation, FDA compliance to the Code of Federal Regulations purported by the Food and Drug Administration, and HIPAA compliance set forth by the Office of Civil Rights.
Contact Information
For information regarding this press release, please contact Michael Gregor at 978-473-9265 or mail us at info@ComplianceDoc.com.
http://www.compliancedoc.com
About ComplianceDoc, Inc.
ComplianceDoc, Inc. is a privately held company that combines extensive software and diverse regulatory compliance experience to provide services and content over the Internet. In addition, our services and content are conveniently accessible and well organized for our users. We are proud to serve the following industries: Cosmetic, Drug, Food, Healthcare, Legal, and Medical Device.
This release was published on openPR.
Permanent link to this press release:
Copy
Please set a link in the press area of your homepage to this press release on openPR. openPR disclaims liability for any content contained in this release.
You can edit or delete your press release Latest version of IndexFDA adds cross-indexed, searchable 21 US Code content here
News-ID: 12048 • Views: …
More Releases for FDA
DreaMed receives 5th FDA Clearance
TEL AVIV, Israel: DreaMed Diabetes LTD. ("DreaMed" or the "Company"), developer of the endo.digital Clinical Decision Support System announced today that it has received its 5th U.S Food and Drug Administration (FDA) clearance that expands the scope of AI enhanced treatment recommendations to patients on fixed meal insulin regimens. endo.digital is the first decision support system that has been cleared to assist healthcare providers in the management of diabetes…
FDA Compliant Blood Storage and Preservation
Accsense Monitoring System Automates Data Archive and Alarming
CAS DataLoggers provided the temperature alarming and monitoring system to a hospital blood bank looking to replace their old paper chart recorders as they became unreliable and spare parts were harder to find. For proper blood storage and preservation, the lab’s medical units needed to maintain storage temperatures between 2°C to 6°C (36°F to 43°F), given the perishability of blood components. The facility…
FDA grants orphan drug status to Vicore
US Food and Drug Administration has awarded Vicore Pharmaceuticals with orphan Drug designation for the treatment of Idiopathic Pulmonary Fibrosis (IPF). FDA’s Orphan Drug Designation program provides certain incentives for companies developing therapeutics to treat rare diseases or conditions, defined as those affecting less than 200,000 individuals in the U.S. A drug candidate and its sponsor must meet several key criteria in order to qualify for, and obtain, orphan drug…
New FDA Design Control Training Courses
Salt Lake City, Utah - February 23 2017 - Procenius Consulting is a medical device consulting firm specializing solely in medical device design controls regulation (21 CFR 820.30).
Announcing New Design Control Training Courses
Procenius Consulting has just launched two new training courses covering basic and advanced topics of medical device design control regulation. These courses focus on compliance, practical implementation and industry best practices techniques for developing or improving a…
fda online training
GRC Training Solutions provides end-to-end FDA compliance solutions for those companies who want to maximize security, minimize operational costs, improve staff productivity and stay on top of all their compliance documentation.
GRC Training Solutions boasts a team of experts and specialists who have a proven track record in working with the biotechnology, medical device, diagnostic and pharmaceutical fields. Our team will work with you closely and develop solutions that meet…
FDA online training
Description:
Device firms, establishments or facilities that are involved in the production and distribution of medical devices intended for use in the U.S are required to register annually. Most establishments that are required to register with the FDA are also required to list the devices that are made there and the activities that are performed on those devices. Initially, FDA issued a 28-page Proposed Rule that would amend its regulations regarding…
