MedTech I.Q.

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All Blog Posts (1,644)

Device Establishment Registration and Listing in line with the FDA’s Proposed Rule

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.…

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Added by Adam Fleming on October 20, 2016 at 5:59am — No Comments

Understanding an audit management system

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Added by Adam Fleming on October 19, 2016 at 5:40am — No Comments

Identifying and resolving common issues in FDA Software Validation & Verification

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.…

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Added by Adam Fleming on October 18, 2016 at 5:50am — No Comments

Fine-tuning biomedical writing brings a number of benefits

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…

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Added by Roger Steven on October 17, 2016 at 6:00am — No Comments

Tightening carrier food safety issues can save costs for the food and logistics industries

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…

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Added by Adam Fleming on October 17, 2016 at 5:53am — No Comments

Practice Managers need to be thorough in their understanding of HIPAA requirements



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…

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Added by Roger Steven on October 14, 2016 at 6:24am — No Comments

Time-saving tips on MS Excel usage

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…

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Added by Adam Fleming on October 14, 2016 at 5:40am — No Comments

Cost-effective regulatory compliance trainings get even more cost-effective!

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.…

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Added by Adam Fleming on October 13, 2016 at 7:00am — No Comments

Adherence to the Anti-Kickback and Stark Law is more than just a compliance issue

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…

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Added by Roger Steven on October 13, 2016 at 5:55am — No Comments

Avoiding punitive actions from the FDA

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.…

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Added by Adam Fleming on October 13, 2016 at 5:32am — No Comments

Understanding HIPAA Compliance Requirements

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…

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Added by Roger Steven on October 12, 2016 at 5:54am — No Comments

The FDA steps up efforts at bringing about medical device cyber security

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Added by Adam Fleming on October 12, 2016 at 5:41am — No Comments

Know the ropes of social media in healthcare to avoid costly penalties from HIPAA

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…

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Added by Roger Steven on October 11, 2016 at 6:34am — No Comments

A look at FDA GMP compliance

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…

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Added by Adam Fleming on October 11, 2016 at 6:10am — No Comments

Preparing for a HIPAA audit

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…

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Added by Roger Steven on October 6, 2016 at 6:17am — No Comments

The FDA code of federal regulations

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…

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Added by Adam Fleming on October 6, 2016 at 5:46am — No Comments

A glance at Good Clinical Practice regulations

Good Clinical Practices are a collectively bunched global scientific, quality and ethical standard relating to the following aspects of a clinical research:

  • Design
  • Conduct
  • Documentation (recording)
  • Report making

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…

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Added 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…

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Added by Worksure Medpharma on October 5, 2016 at 5:35am — No Comments

Ensuring quality at every point of the food transportation chain is crucial for ensuring public health

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.…

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Added by Adam Fleming on October 4, 2016 at 7:31am — No Comments

Healthcare computer systems implementation involves choosing the right method

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…

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Added by Roger Steven on October 3, 2016 at 6:00am — No Comments

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