Health Canada switches to mainly pharmaceutical funding

[impact]

Notice the date this occured. The influence from Big Pharma can no longer be denied.

February 13, 2018 By DATAC

In October of last year, Health Canada announced that it would be raising the fees it charges to drug manufacturers for new medicines introduced into the market. Historically, Health Canada has used these fees to fund 50% of its operating costs in regulating prescription medication, but plans to raise this to 90% with the coming fee increase. It also plans to provide a 24% rebate if it fails to review new drug applications within the accepted time frame.

Before user fees were introduced in 1994, Health Canada was entirely funded by tax dollars. Now, with the majority of its funding arising directly from the pharmaceutical industry, questions have been raised about whether or not the goal of drug companies to sell their products in vast quantities poses a conflict of interest with Health Canada’s responsibility to provide safe and effective drugs to Canadians.


While many argue that a faster process to review drugs allows the public earlier access to new medicines, there is no evidence that this pressurized approach benefits public health. In fact, most drugs newly approved in Canada are no safer or more effective than those already on the market; between 2010-2016, only 10.6% of newly patented drugs were identified as a substantial improvement or breakthrough when compared to what was already available to consumers.
In addition, faster review times for new drugs can impact the safety of the product. Typically, drugs reviewed within 300 days have a 20% chance of requiring new safety warnings, while this percentage rises to 33% when the review period is shortened to 180 days.
Additionally, instituting rigid review timelines for the sake of speed can impact public safety. In the USA, products approved within the FDA’s sixty day deadline are five times more likely to be withdrawn from the market due to safety concerns, and four times more likely to include serious safety warnings.
As pressure grows to meet regulation board deadlines, reviewers can miss or overlook safety concerns, which poses a great concern to critics of Health Canada’s decision to fund the majority of its regulation operating cost through the private pharmaceutical sector.



https://datac.ca/health-canada-switc...tical-funding/

[410001661]

Notice the date this occured. The influence from Big Pharma can no longer be denied.

February 13, 2018 By DATAC

In October of last year, Health Canada announced that it would be raising the fees it charges to drug manufacturers for new medicines introduced into the market. Historically, Health Canada has used these fees to fund 50% of its operating costs in regulating prescription medication, but plans to raise this to 90% with the coming fee increase. It also plans to provide a 24% rebate if it fails to review new drug applications within the accepted time frame.

Before user fees were introduced in 1994, Health Canada was entirely funded by tax dollars. Now, with the majority of its funding arising directly from the pharmaceutical industry, questions have been raised about whether or not the goal of drug companies to sell their products in vast quantities poses a conflict of interest with Health Canada’s responsibility to provide safe and effective drugs to Canadians.


While many argue that a faster process to review drugs allows the public earlier access to new medicines, there is no evidence that this pressurized approach benefits public health. In fact, most drugs newly approved in Canada are no safer or more effective than those already on the market; between 2010-2016, only 10.6% of newly patented drugs were identified as a substantial improvement or breakthrough when compared to what was already available to consumers.
In addition, faster review times for new drugs can impact the safety of the product. Typically, drugs reviewed within 300 days have a 20% chance of requiring new safety warnings, while this percentage rises to 33% when the review period is shortened to 180 days.
Additionally, instituting rigid review timelines for the sake of speed can impact public safety. In the USA, products approved within the FDA’s sixty day deadline are five times more likely to be withdrawn from the market due to safety concerns, and four times more likely to include serious safety warnings.
As pressure grows to meet regulation board deadlines, reviewers can miss or overlook safety concerns, which poses a great concern to critics of Health Canada’s decision to fund the majority of its regulation operating cost through the private pharmaceutical sector.



https://datac.ca/health-canada-switc...tical-funding/

Newly patented drugs are not always new drug compounds recently developed. Patents for drugs are only 7 years and the clock starts ticking once the drug reaches trials (testing on target demographics), so it could take a couple of years for trials to end leaving only 5 years of patent to re-coup the R&D investment. What a pharma company can do is use an existing compound that is still under patent, and if they have supporting data that it looks promising for another cure then they can enter trials for that other cure and the patent gets re-newed.

You have to remember that drug approval by Health Canada usually takes into account the efficacy of that drug on that target demographic but also takes into account the cost of that drug in that treatment. There are some amazing drugs on the market that are not approved by health Canada and it has nothing to do with the efficacy of that compound it is a business decision. This is why you see people going to the US for some cancer treatment.

[NJohnson]

They are all crooks starting with FDA influencing Health Canada

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[smitty55]

They are all crooks starting with FDA influencing Health Canada

Speaking of the FDA

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