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The FDA grants marketing approval for certain types of medical products whose application is the result of foreign clinical studies, provided the products and the clinical studies meet certain conditions. The types of medical products…

Added by John Robinson on December 11, 2017 at 5:41am — No Comments
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Added by John Robinson on December 8, 2017 at 5:40am — No Comments
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Added by John Robinson on December 7, 2017 at 6:45am — No Comments
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Added by John Robinson on December 6, 2017 at 5:53am — No Comments
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Added by John Robinson on December 5, 2017 at 6:08am — No Comments
Export, import and trade compliance principle is a very important guiding standard for governing trade policies and ensuring compliance with the set national, regional and global trade norms. It helps to define an organization’s adherence to the export, import and trade compliance principle laid out by the government and also offers an…
Added by John Robinson on December 4, 2017 at 4:50am — No Comments
In the world of commerce, internet is king as it never sleeps and continues to take transactions long after you and I have laid to rest for the night. With the evolution of finance and online transactions the internet world has taken large steps to make it easier for the consumer and investor to feel more safe and secure with the funds which are being processed.
Remember when Paypal came on the scene? “E-commerce”? It was still like a toddler –…
Added by Adam Fleming on December 1, 2017 at 5:11am — No Comments

A signal is described by the World Health Organization as any information that is reported on a possible or potential causal relationship between a drug and the adverse event it spawns. This relationship can be of virtually any nature, so long as it concerns the drug and the…
Added by John Robinson on December 1, 2017 at 4:35am — No Comments

There are various core components of a financial audit program. First, an understanding of a financial audit:
Added by John Robinson on November 30, 2017 at 5:37am — No Comments

Logistics and supply chain management (SCM) constitute a very important element of businesses. Getting the logistics and supply chain management aspects right is necessary for the smooth flow of products from their source to destination, during the course of which many activities need to be performed.
Logistics and supply chain management is emerging as a…
Added by John Robinson on November 29, 2017 at 4:53am — No Comments

The adverse event reporting system is an important highlight of the FDA’s adverse event reporting requirements. This is the mechanism through which adverse event reporting requirements are listed out for the FDA to take further action.
The adverse event reporting system may be understood as being a database…
Added by John Robinson on November 28, 2017 at 5:43am — No Comments
Pharmaceutical Process Engineering is an often-overlooked area in the field of pharmaceutical manufacturing. It calls for a high degree of precision and coordinates technical expertise and communication between professionals involved at diverse levels of the manufacturing unit, such as pharmaceutical researchers, chemical engineers and industrial. It is concerned with how pharmaceutical development is related to the application of major concepts and…
Added by Adam Fleming on November 28, 2017 at 5:30am — No Comments
The internal audit checklist for HIPAA is one of the primary elements of HIPAA implementation. The passage of the Health Insurance Portability and Accountability Act (HIPAA) by the U.S. Congress in 1996 was aimed at regulating the way and process by which healthcare institutions across the country reveal the medical information of their patients.
The Department of…
ContinueAdded by John Robinson on November 24, 2017 at 4:45am — No Comments
Medical devices and drugs clinical research have their differences in approach and methodology. It is necessary to have a clear understanding of these differences if one embarks upon a study involving either or both of these.
Some of the major differences between device and drug clinical research include:
Requirement for a study:
One of the important differences between device and…
ContinueAdded by Roger Steven on November 23, 2017 at 6:16am — No Comments
The new chief of the Philippines’ anti-drug agency has promised a fresh approach to the controversial war on drugs, “based on the rule of law”.
Aaron Aquino said that since he took over in August, only one suspect had been killed in 1,341 operations.
Thousands have died in the anti-drug campaign since it was launched by President Rodrigo Duterte in 2016.
Rights groups say Mr Duterte has sanctioned extrajudicial killings by vigilantes…
Added by Adam Fleming on November 23, 2017 at 4:55am — No Comments
The most critical aspect of risk management is the identification of potential areas of risk management. This helps the organization to stay focused on the areas in which it could possibly face risks, rather than taking an aimless view and shooting about in the dark.
In a very broad sense, the potential areas of risk management include all areas of a business, because simply…
ContinueAdded by John Robinson on November 23, 2017 at 4:41am — No Comments
With over four million employed directly or in allied sectors and catering to the world’s largest market and research area, biotech and pharma is a fast growing industry. Its courses are designed to prepare individuals for this giant industry.
Biotech and pharmaceutical courses are much sought after by aspiring…
Added by John Robinson on November 22, 2017 at 5:09am — No Comments

Auditing Quality Management Systems is a core requirement for ensuring that Quality Management Systems – defined as “…a set of policies, processes and procedures required for planning and execution” in the core business area of an organization, meaning those that impact the ability of the organization to meet…
Added by John Robinson on November 21, 2017 at 5:20am — No Comments
Good Manufacturing Practices (GMPs) constitute one of the core components that go into the manufacture and distribution of foods, drugs and other pharmaceutical products. Good Manufacturing Practices are prescribed by regulatory agencies from around the world, the FDA and the EMA being among them.
The guidelines set out by these regulatory…
Added by John Robinson on November 20, 2017 at 5:22am — No Comments
The US economy’s appetite for ingesting food imports is phenomenal, to use a mild term. How else does one describe an economy that takes in $49 billion a year? Considering that the FDA is the sole regulating agency that is tasked with overseeing imports of this magnitude, who can envy its responsibility? This is not all that the FDA does: its allied regulatory agencies monitor about half a million facilities in the US and abroad.
Since foods from…
Added by Adam Fleming on November 17, 2017 at 5:23am — No Comments
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