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Examples of product demo videos
Businesses have been producing videos from ages, we know them as Ads. In past 5 years businesses have invested in marketing themselves online and at the top of the pyramid video marketing is proving to have a huge impact. Product demo videos are used to showcase the key info about the product and its benefits
Here are some examples of …
ContinueAdded by Richard Walter on January 17, 2017 at 6:57am — No Comments
3D animation video examples
How your organization or you might choose to use 3D Animated Videos varies a lot, but due to its great output and look & feel its a preferred medium to create videos. For creating quality 3D video content choose a video production company who has a good portfolio and is also flexible in working with your requirements
Here are some examples of …
ContinueAdded by Richard Walter on January 17, 2017 at 6:48am — No Comments
2d video production examples
How your organization or you might choose to use 2D Animated Videos varies a lot, but due to its low cost and fast turn around time its a preferred medium to create videos. For creating quality 2D video content choose a video production company who has a good portfolio and is also flexible in working with your requirements.
Here are some examples of …
ContinueAdded by Richard Walter on January 17, 2017 at 6:40am — No Comments
Compliance for medical devices is a very broad and vast topic. When one talks of compliance for medical devices, one needs to keep in mind the various regulations that the FDA has put in place for manufacturers of medical devices to comply with. The FDA requires strict compliance with its laws and requirements because it is charged with the task of ensuring…
ContinueAdded by John Robinson on January 16, 2017 at 5:46am — No Comments
ISO 14971:2012 and IEC 62304:2006 are related but different global standards for risk management pertaining to software used in medical devices. Judicious application of these two standards is the way to go for medical device companies.
ISO 14971 and IEC 62304:2006 are global standards that govern risk management and lay out regulations and guidelines for…
ContinueAdded by John Robinson on January 13, 2017 at 4:54am — No Comments
Japan is the world's third largest market for medical devices, after the US and Europe. Ironically, many of the world's medical device manufacturers find language barriers for communicating with Japanese regulatory authorities a greater barrier than passing through the regulatory maze! The regulatory filing requirements for medical devices in Japan are…
ContinueAdded by John Robinson on January 12, 2017 at 4:51am — No Comments
Medical device reporting and recalls have enormous benefits for the medical device company and the public if implemented properly. They can prevent use…
ContinueAdded by John Robinson on January 11, 2017 at 5:01am — No Comments
Though short in length,HIPAA Security Rule principles are well defined in some areas, but vague in some others, making implementation of these areas difficult.
HIPAA Security Rules are an offshoot of the Privacy Rule. While Privacy Rule concerns itself with Protected Health Information (PHI) in general, the HIPAA Security Rule (SR) concerns itself…
ContinueAdded by John Robinson on January 10, 2017 at 4:45am — No Comments
In order to ensure GMP compliance, pharmaceutical laboratories have to devise a holistic and long term plan that covers all aspects of the laboratory's activities.
Good Manufacturing Practices (GMP) requirements for laboratories have been set out by various regulatory bodies. The aim of GMP compliance for a pharmaceutical laboratory is to ensure…
ContinueAdded by John Robinson on January 9, 2017 at 6:00am — No Comments
Software Validation Process for 21 CFR Part 11 is all about authenticity and integrity of electronic signatures and records. Care should be taken to avoid confusion and get validation right.
The FDA’s Code of Federal Regulations (CFR) is a collection of laws that regulate the various government agencies. Different titles of the CFR govern respective regulated…
ContinueAdded by John Robinson on January 6, 2017 at 4:35am — No Comments
In July 2010, the Obama administration chalked out new Electronic Health Record Standards. These Electronic Health Record Standards were a major improvisation on the standards that existed till then. The idea behind revising the existing Standards is to…
Added by Roger Steven on January 4, 2017 at 7:00am — No Comments

A HIPAA audit is very important for service providing organizations, because the penalties for violations can bring their business down. It is important to understand the nuances of a HIPAA audit if one has to be successful.
A HIPAA audit is, for many service providing organizations, a make or break situation. This is because HIPAA audits are considered stringent. Violations can attract huge penalties, which is why getting it right the first time is extremely…
ContinueAdded by Roger Steven on December 9, 2016 at 4:20am — No Comments

For many professionals, writing skills are learned while they are on the job. In many cases, they would go by a preferred style or other documents or style guides that help to put a certain style in place. Editing, however, is rarely taught. Worse, the perception most people have of editing is that it is revising or rewriting a work. But the truth is different. Editing gives shape to a document. It helps to perfect and sculpt it. The big question most editors face…
ContinueAdded by Roger Steven on November 29, 2016 at 6:10am — No Comments
Financial institutions have long been the most important source of payments for their customers. Of late, though, with an increase in competition and the advent of new non-bank entries into the marketplace, financial institutions have come under a lot more strain than they used to be.

Financial institutions need to reinvent themselves in a number of ways. They need to adapt novel strategies to…
ContinueAdded by Adam Fleming on November 25, 2016 at 5:03am — No Comments

Nanotechnology, a part of Quantum Physics (QP), is growing fast and has myriad uses. Nanotechnology is all about size and self-assembly. While QP deals with subatomic particles and waves; Nano relates to the atomic and molecular level. Atomic behavior and properties get dramatically changed at the Nano level. Of note are properties such as color change due to refraction of light. Gold, packaging and chemistry are some of the well-known areas into which…
ContinueAdded by Roger Steven on November 25, 2016 at 4:50am — No Comments
Compared to bigger actions, Recalls, 483s, Warning Letters and consent decrees are only some of the milder parts of punishments that the FDA could impose on a medical device company that fails to meet regulatory requirements. The bigger actions can include seizure, injunction, and civil money penalties. The Park Doctrine allows executives to even be sentenced to prison.

In the…
Added by Adam Fleming on November 22, 2016 at 4:50am — No Comments
Food establishments continue to be a major source for pests due to the changes brought about in the means and ways by which food is produced and handled and in the ways of preparation techniques and eating habits. The pests in turn are sources for illness-causing microorganisms. The more knowledge about pest control at their disposal; the better it is for food processing and foodservice personnel, because this is essential for ensuring a safe food supply for consumers.…
Added by Adam Fleming on November 17, 2016 at 4:43am — No Comments
For those in the field of exploration, there is a need to zero in on an effective and affordable methodology that identifies prospective targets which are related to, or controlled by tectonic structures. This methodology should help explorers concentrate their exploration efforts over new areas keeping their budget in control, armed even with limited or nonexistent geological information.…
Added by Adam Fleming on November 16, 2016 at 4:47am — No Comments

The importance of conducting a risk analysis updating it can be gauged from the fact that failure to conduct a written risk analysis qualifies as “willful neglect”, which carries the highest Civil Money Penalty (“CMP”). This cannot be waived by the DHHS unlike violations that happen due to a reasonable cause.
Since risk analysis is a required implementation specification under the Security Rule, failure to do one amounts to willful neglect. If the civil…
ContinueAdded by Roger Steven on November 15, 2016 at 5:23am — No Comments
That the FDA has become more rigorous in the enforcement of Part 11 through its new Part 11 and on-going data integrity inspection and enforcement program is evident in this: In just the last three years, it issued more than 30 Warning Letters with Part 11 and data integrity violations. The most common citations are related to not only inadequate integrity, security and availability of electronic records, but also to validation of software and computer systems.…
Added by Adam Fleming on November 15, 2016 at 4:44am — No Comments
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