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Other important factors related to ED include improved quality of life and partnership support. In addition to treatment, communication and support with partners play a major role in overcoming EDs. Another notable aspect is the increasing accessibility of treatment due to the proliferation of online and remote treatment.

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To export drugs from India to EU.

Exporting drugs from India to Europe requires some special licensing and regulatory compliance. This includes not only the regulatory requirements of the exporting country, India, but also those of the importing country, the European Union. The main steps and requirements are described below. Regulatory Requirements in India European Union (EU) Regulatory Requirements European Medicines Agency (EMA) The European Medicines Agency (EMA) evaluates and monitors medicines for all member states of the European Union (EU).The EEA includes the EU member states as well as Norway, Iceland,...

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FDA Licensing in India

In order to obtain and maintain an FDA license in India, it is important to understand the Indian regulatory environment. The term “FDA” in India usually refers to the Central Drugs Standard Control Organization ( CDSCO ), which is the primary agency under the Indian Ministry of Health and Welfare that regulates the quality, safety, and efficacy of drugs and medical devices under the Indian Ministry of Health and Welfare. FDA Licensing Process License Maintenance Obtaining and maintaining an FDA license in India is a...

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Is there an invisible tax on brand-name drugs?

The expression ” brand-name drugs include an invisible tax ” is not commonly used to describe drug prices, but to understand what is being referred to, let us consider the composition of drug prices. Composition of drug prices Interpreting “Invisible Taxes” Conclusion The main reason for the high price of brand-name drugs is the need to recover R&D and other costs. While there is no direct “invisible tax” included in the price, it is true that expensive R&D costs are reflected in the price. Some...

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Domestic brand-name products are not superior.

While it is true that opinions exist regarding the choice of drugs, such as “brand-name products are better” or “domestic products are better,” there are several reasons for this, but they do not necessarily apply to everyone. Here are a few points to consider Original and Generic Products Domestic and imported products Conclusion While “brand-name drugs are better” or “domestically made drugs are better” reflects a general expectation of reliability and quality, generics are also basically considered reliable in terms of safety and effectiveness since...

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Is maca a placebo effect?

It is important to consider the placebo effect with respect to maca. In particular, it is necessary to distinguish between actual physiological effects and placebo effects (the phenomenon of feeling an effect simply because you believe in it ) when evaluating effects on supplements. What is the Placebo Effect? The placebo effect refers to the phenomenon of improvement that occurs even when a “placebo” is used that does not contain an active ingredient. This effect often occurs because of the patient’s expectation that he or...

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To split tadalafil in half.

Tadalafil (Tadalafil) is a medication used to treat erectile dysfunction and prostate enlargement, and its trade names include Cialis. Several points should be considered regarding the appropriateness of splitting this medication in half. Notes on splitting tadalafilTablet type: Notes on splitting tadalafil Tablet type: Tadalafil may contain film-coated tablets. This type of tablet may be divided in half, which may change the effectiveness of the drug, because the coating may control the absorption of the drug. The presence or absence of a coating is often...

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Recommendations from IFPMA

OverviewThe World Health Organization (WHO) defines a counterfeit drug as “a medicine that intentionally/fraudulently misrepresents its identity, composition, or source.” Overview The World Health Organization (WHO) defines a counterfeit drug as “a medicine that intentionally/fraudulently misrepresents its identity, composition, or source.” Quality counterfeit medicines do not exist and the manufacture, distribution and sale of counterfeit medicines is a crime. We are at the forefront of the fight against counterfeit medicines that endanger the lives of people in all countries who need medicines. The Growing Threat...

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Why are so many generic drugs manufactured in India?

India’s drug patent laws have features that have attracted international attention. In relation to why India is a major producer of generic drugs, below is a description of its laws and the background behind its ability to produce drugs at low cost. Features of Indian Patent Law India enacted the Indian Patents Act of 1970.This law reflects India’s decision to adopt a unique approach to developing its industry, although it was significantly amended in 2005 to comply with the World Trade Organization’s (WTO) TRIPS Agreement...