The Cutting Edge of Medical Technology Content, Community & Collaboration
Annual registration is a requirement for any device firm, establishment or facility whose business relates to the production and distribution of medical devices intended for use in the US in some or another way.

Such business establishments have to register with the FDA and also need to list the devices that are made there and the activities that are performed on those devices.…
Added by Adam Fleming on October 20, 2016 at 5:59am — No Comments
An audit management system can be understood as a set of audit systems that an organization puts in place to ensure that it meets its objectives. All organizations need to have their own audit management systems. An audit management system is a system that facilitates the management of…
Added by Adam Fleming on October 19, 2016 at 5:40am — No Comments
Verification and Validation (V & V) are two important aspects of regulatory compliance for software. What all are needed for achieving this? The FDA, GAMP and others provide guidance in the methodology and documentation needed for this. This apart; consideration of the principles in ISO 14971 can assist in providing an acceptable vehicle by which to perform and document risk-based software V&V.…
Added by Adam Fleming on October 18, 2016 at 5:50am — No Comments
A very big misconception in the field of medicine is that biomedical writing is highly technical and replete with jargon, and therefore not creative. There is enough scope in biomedical writing for creativity and the use of artistic and imaginative words without compromising on the meaning or import of the words. In fact, resorting to the use of imaginative words…
ContinueAdded by Roger Steven on October 17, 2016 at 6:00am — No Comments
A good portion of the current recall and shipment rejection issues happen within the cold chain food transportation sector, resulting in fairly high, but preventable financial loss. This is an indication of how much scope is there to contain seepage in the food and transportation industries.

Is this happening because of lack of regulation? No. Rather, it is the lack of proper…
Added by Adam Fleming on October 17, 2016 at 5:53am — No Comments
Practice managers, business managers and compliance officers need to have all their points in order before a HIPAA audit. They need to be fully educated about the misconceptions and realities of a HIPAA audit, since there is a lot of misinformation about HIPAA that keeps doing the rounds most of the time. These professionals who deal with HIPAA audits for their…
Added by Roger Steven on October 14, 2016 at 6:24am — No Comments
MS Excel is a program that has an amazing number of features that make it highly capable and suited for a number of usages. Although it has innumerable features; they come with simple shortcuts and methods. These are not always visible to the casual user. The use of these shortcuts is of tremendous use to users, because it saves them precious time, which can be put to more valuable uses. Employees who know the secrets of MS Excel are certainly likely to be more…
Added by Adam Fleming on October 14, 2016 at 5:40am — No Comments
There are offers, and then there are super offers. Finally, there are Compliance4All offers! Yes, Compliance4All has an offer that is so unique that it can be considered a step above being a super offer. What is this offer, then? Compliance4All, a leading provider of professional trainings for all the areas of regulatory compliance, has just announced that it is offering a 50% off on its webinar packs. Wait. Don’t rush for your reading glasses. You’ve read it right.…

Added by Adam Fleming on October 13, 2016 at 7:00am — No Comments
The Anti-Kickback and Stark Law is a vital Act for healthcare practitioners, and it includes several changes for 2016.
Is the implementation of the Stark Law important? It is much more than being just important. It is critical. The reason for this is that lack of proper implementation of this law in its entirety attracts substantial awards and settlements, as…
ContinueAdded by Roger Steven on October 13, 2016 at 5:55am — No Comments
Although the news of a company receiving strictures from the FDA in the form of 483s, Warning Letters, and even Consent Decrees is a near daily occurrence in the industry; when it happens, it takes such companies by surprise. Not only is the company’s executive management caught off guard by these events; they are also embarrassed by the bad press they get, as well by the very expensive and damaging investigations and corrective and preventive action that follow.…
Added by Adam Fleming on October 13, 2016 at 5:32am — No Comments
An organization that needs to be HIPAA compliant has to not only ensure that it provides the appropriate patient rights and controls on its uses and disclosures of Protected Health Information (PHI); it has to also have the proper policies and procedures in place. Any organization that is the subject of a compliance review or is being audited has to demonstrate to the government that it has both the documentation necessary for safeguarding patient PHI, as well as the ability to show…
ContinueAdded by Roger Steven on October 12, 2016 at 5:54am — No Comments
It is a disturbing, but true fact that medical devices are hacked. Medical devices have inbuilt software, and hackers try to breach this. Medical device cyber security is thus critical, because lack of it can bring harm to patients who use medical devices that come with software built…
Added by Adam Fleming on October 12, 2016 at 5:41am — No Comments
Any healthcare organization that is active on the social media is vulnerable to some or another kind of Protected Health Information (PHI) breach. Although a healthcare practice or business benefits greatly in terms of marketing and publicity from the judicious use of the social media for; data stored on Facebook, LinkedIn, YouTube or Instagram leaves it susceptible…
ContinueAdded by Roger Steven on October 11, 2016 at 6:34am — No Comments
In a broad sense, GMPs refer to good manufacturing practices in any field. The main intention of these GMPs is that they enable industries to perform the required practices needed for complying with guidelines set out by the regulatory authorities. GMP guidelines are issued by regulatory authorities all around the world, mainly in the US, Canada, the countries of Europe and many others.

The ambit…
ContinueAdded by Adam Fleming on October 11, 2016 at 6:10am — No Comments
An organization that needs to be HIPAA compliant has to not only ensure that it provides the appropriate patient rights and controls on its uses and disclosures of Protected Health Information (PHI); it has to also have the proper policies and procedures in place. Any organization that is the subject of a compliance review or is being audited has to demonstrate to…
ContinueAdded by Roger Steven on October 6, 2016 at 6:17am — No Comments
FDA Code of Federal Regulations (CFR) is a huge sea of regulations that the FDA has created for regulating all products that come under its purview of regulation. The FDA codes of federal regulations are numbered and cover all products, processes and the activities that go into their creation.

The FDA Code of Federal Regulations is a compendium of codified general and permanent rules the federal…
ContinueAdded by Adam Fleming on October 6, 2016 at 5:46am — No Comments
Good Clinical Practices are a collectively bunched global scientific, quality and ethical standard relating to the following aspects of a clinical research:

Relevant Good Clinical Practice regulations are to be followed by the sponsors of a clinical trial, no matter how big or small the trial or…
ContinueAdded by Adam Fleming on October 5, 2016 at 6:37am — No Comments
Role of CROs in improving knowledge productivity in health care industry
Contract research organisation (CRO) is a fastest growing segment, provides support to pharmaceutical, biotechnology and medical device industries in the form of research services. The pharmaceutical companies can’t uphold and drop billions due to termination of patent and deficiency of new approvals. So they are approaching strategic alliances to sustain revenue and improve the product pipelines. These companies are increasingly…
ContinueAdded by Worksure Medpharma on October 5, 2016 at 5:35am — No Comments
Whenever food, either in raw form or after being cooked, is transported, it carries the risk of contamination. Since the food that is being transported is so vulnerable, care has to be taken at just about every possible point in order to prevent disease from originating and spreading from the sources of food transporation. Standard procedures for washing and sanitizing the containers, in which food is transported need to be established, managed and maintained.…
Added by Adam Fleming on October 4, 2016 at 7:31am — No Comments
Healthcare computer systems implementation can be anything from a headache to nightmare, given its complexity. Things can go wrong at any stage and for any reason. Getting the computer systems right or implementing the right one involves investment of considerable time and money from all kinds of healthcare organizations, big or small.
Fortunately, many of…
ContinueAdded by Roger Steven on October 3, 2016 at 6:00am — No Comments
2026
2025
2024
2022
2020
2019
2018
2017
2016
2015
2014
2013
2012
2011
2010
2009
2008
1999
© 2026 Created by CC-Conrad Clyburn-MedForeSight.
Powered by