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November Newsletter 2024 – Chinese Traditional

We look forward to sharing the latest updates and insights in our November Newsletter 2024 – Chinese Traditional. What’s inside in November Newsletter 2024 – Chinese Trad...
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November Newsletter 2024 – Chinese Simplified

We look forward to sharing the latest updates and insights in our November Newsletter 2024 – Chinese Simplified. What’s inside in November Newsletter 2024 – Chinese Simpl...
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November Newsletter 2024 – Japanese

We look forward to sharing the latest updates and insights in our November Newsletter 2024 – Japanese. What’s inside in November Newsletter 2024 - Japanese? 1. The lates...
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November Newsletter 2024 – Korean

We look forward to sharing the latest updates and insights in our November Newsletter 2024 – Korean. What’s inside in November Newsletter 2024 - Korean? 1. The latest in...
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November Newsletter 2024

We look forward to sharing the latest updates and insights in our November Newsletter 2024. What’s inside in November Newsletter 2024? 1. The latest information on me...
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October Newsletter 2024 – Japanese

We look forward to sharing the latest updates and insights in our October Newsletter 2024 – Japanese. What’s inside in October Newsletter 2024? 1. The latest information...
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October Newsletter 2024 – Simplified Chinese

We look forward to sharing the latest updates and insights in our October Newsletter 2024 – Simplified Chinese. What’s inside!! 1. The latest information on medical...
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October Newsletter 2024 – Traditional Chinese

We look forward to sharing the latest updates and insights in our October Newsletter 2024 – Traditional Chinese. What’s inside!! 1. The latest information on medica...
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October Newsletter 2024 – Korean

We look forward to sharing the latest updates and insights in our October Newsletter 2024 - Korean. What’s inside in October Newsletter 2024? 1. The latest information on&...
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October Newsletter 2024

We look forward to sharing the latest updates and insights in our October Newsletter 2024. What’s inside in October Newsletter 2024? 1. The latest information on medi...
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September Newsletter 2024 – Simplified Chinese

We look forward to sharing the latest updates and insights in our September Newsletter 2024 – Simplified Chinese. What’s inside!! 1. The latest information on medic...
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September Newsletter 2024 – Korean

We look forward to sharing the latest updates and insights in our September Newsletter 2024 – Korean. What’s inside!! 1. The latest information on medical device re...
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September Newsletter 2024 – Japanese

We look forward to sharing the latest updates and insights in our September Newsletter 2024 – Japanese. What’s inside!! 1. The latest information on medical device...
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September Newsletter 2024 – Traditional Chinese

We look forward to sharing the latest updates and insights in our September Newsletter 2024 – Traditional Chinese. What’s inside!! 1. The latest information on medi...
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September Newsletter 2024

We look forward to sharing the latest updates and insights in our September Newsletter 2024. What’s inside in September Newsletter 2024? 1. The latest information on ...
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August Newsletter 2024 – Korean

We look forward to sharing the latest updates and insights in our August Newsletter 2024 – Korean What’s inside!! 1. The latest information on medical device regula...
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August Newsletter 2024 – Simplified Chinese

We look forward to sharing the latest updates and insights in our August Newsletter 2024 – Simplified Chinese. What’s inside!! 1. The latest information on medical...
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August Newsletter 2024 – Traditional Chinese

We look forward to sharing the latest updates and insights in our August Newsletter 2024 – Traditional Chinese. What’s inside!! 1. The latest information on medical...
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August Newsletter 2024 – Japanese

We look forward to sharing the latest updates and insights in our August Newsletter 2024 - Japanese. What’s inside!! 1. The latest information on medical device regulation...
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August Newsletter 2024

We look forward to sharing the latest updates and insights in our August Newsletter 2024. What’s inside in August Newsletter 2024? 1. The latest information on medical de...
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Five minute reads

KIMES Busan Medical & Hospital Equipment Show

The KIMES Busan Medical & Hospital Equipment Show is a premier event in South Korea’s medical industry, showcasing the latest advancements in medical technology, hospital equipment, and healthcare solutions. Held annually i...

Cosmetic Blogs

The UK has specific regulations governing the safety, labelling, and marketing of cosmetic products. Post-Brexit, the UK has its own regulatory framework separate from the EU. UK Cosmetics Requirements &am
Cosmetic Regulatory Requirements in Finland complies with the EU regulation (Regulation (EC) No 1223/2009) without additional national requirements. Finnish Safety and Chemicals Agency (Tukes) In Finland
Cosmetic Regulatory Requirements in Luxembourg complies with the EU regulation (Regulation (EC) No 1223/2009) without additional national requirements specific to cosmetics. The regulation sets out stringent r
In Sweden, cosmetic products are regulated primarily under the framework of the European Union (EU) legislation, specifically Regulation (EC) No 1223/2009 on cosmetic products. This regulation ensures the safe
In the United Kingdom (UK), cosmetic products are regulated under the UK Cosmetics Regulation 2019, which governs the safety and marketing of cosmetic products. This regulation largely mirrors the European Uni
Cosmetic Regulatory Requirements in Belgium follows the EU regulation (Regulation (EC) No 1223/2009) without additional national requirements for cosmetics. Federal Agency for Medicines and Health Products
Cosmetic Regulatory Requirements in France are regulated under European Union (EU) legislation, specifically Regulation (EC) No 1223/2009 on cosmetic products. The French National Agency for Medicines and Heal
Cosmetic Regulatory Requirements in Norway are regulated under the framework of the European Economic Area (EEA) agreement, which aligns Norwegian regulations closely with those of the European Union (EU). The
Spain follows the European Union (EU) regulations for cosmetics, primarily governed by Regulation (EC) No 1223/2009. This regulation ensures the safety and compliance of cosmetic products marketed within the E
Cosmetic Regulatory requirements in Denmark adheres to the EU regulation (Regulation (EC) No 1223/2009). The Danish Environmental Protection Agency (EPA) is the responsible authority for cosmetic regulations a
Italy adheres to the EU regulation (Regulation (EC) No 1223/2009). The Italian Ministry of Health oversees the regulation of cosmetic products in the country. Italian Ministry of Health In Italy, the ove
Poland regulates cosmetic products under the framework of the European Union (EU) legislation, specifically adhering to Regulation (EC) No 1223/2009 on cosmetic products. This regulation ensures the safety and
Understanding the distinctions between product classes within the European cosmetics landscape can be complex and ambiguous, often requiring input from authoritative bodies. Certain products may share simi
In recent years, the beauty and cosmetics industry has witnessed exponential growth worldwide, breaking down geographical barriers and creating a global marketplace. One country that has embraced this trans
eCTD-an overview In today’s economy, life science companies are seeking for strategies to continue growing despite impending patent expirations, increasing generic competition, and rising drug development
The term “animal testing” refers to procedures carried out on living animals for research into basic biology and diseases, evaluating the efficacy of new pharmaceuticals, and testing the safety of consumer
Cosmetic ingredients and products are not required to have FDA clearance before being sold in the U.S. The only exception is colour additives, which need to be authorised for their intended purpose (apart from
Title 21 of the Code of Federal Regulations (CFR), section 7.3(g), describes a recall as a firm’s removal or correction of a marketed product that FDA judges to be in violation of the laws we administer and
by OMC Medical | Dec 13, 2023 | Cosmetics, EU Understanding the distinctions between product classes within the European cosmetics landscape can be complex and ambiguous, often requiring input from au

Pharma Blogs

UK Cosmetics Requirements and Registration Process

The UK has specific regulations governing the safety, labelling, and marketing of cosmetic products. Post-Brexit, the UK has its own regulatory framework separate from the EU. UK Cosmetics Requirements & Registration Proc...

Pharma Blogs

TFDA Requirements for Summary Product Characteristic (SPC) Name of the Medical Product&nbs
The Indonesian Food and Drug Authority (BPOM) plays a crucial role in ensuring the safety and effic
Territory Southeast Asia  Official Language Indonesian/English  Regulatory Authority
MoH: Armenia Ministry of Health MoH website: https://www.gov.am/en/structure/1/ Reg
MoH Ministry of Public Health MoH Website https://moph.gov.af/en Regulatory Authority
A medical device’s intended use and inherent risks must be considered when determining its MDR cl
Technical documentation should contain details of the medical device in a clear, organized, readily
“Professional use” Test Kit – Procedure for registration in UK  Novel Corona Virus Di
Labelling Requirements – Swiss Authorized Representative Written, printed, or graphic informat
Ministry of Health     Ministry of Health Regulatory Authority      National Agen
A medical device’s intended use and inherent risks must be considered when determining its MDR cl
Navigating Medical Device Registration with Iraq’s Regulatory Authority: KIMADIA Guidelines and R
“Professional use” Test Kit – Procedure for Registration in UK  Novel Corona Virus Diseas
South Korea has emerged as a significant player in the global medical device market, and its growth
The UK has specific regulations governing the safety, labelling, and marketing of cosmetic products

Medical Device and IVD Blogs

Switzerland Authorised Representative

Medical devices are regulated by the Swiss Agency for Therapeutic Product Manufacturer Responsibility 1.Ensuring medical devices are placed on the market is in accordance with the requirement of the
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Switzerland Medical Device Regulations

Switzerland Market Situation As the Institutional Agreement is missing (InstA) is missing, the EU has not updated the Mutual Recognition Agreement (MRA) No barrier-free access to the EU internal market
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Swiss Regulation QA WHITE PAPER

MEDICAL DEVICE REGULATION UPDATE IN SWITZERLAND 1. Who is responsible for medical device regulation in Switzerland? The Swiss Agency regulates medical devices for Therapeutic Products (Swiss medic) 2.
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Switzerland AR Responsibilities

Obligations of the Switzerland AR Responsibilities 1. Verify the DoC and technical documentation have been drawn up and where necessary conformity assessment procedure has been carried out. 2. Keep avail
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Swiss Manufacturer Obligations

1. Manufacturers outside Switzerland will need to appoint Swiss AR. 2. The Manufacturer will use commercially reasonable efforts to update its technicaldocumentation for the devices, to comply with the requ
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Labelling Requirements – Swiss Authorized Representative

Labelling Requirements – Swiss Authorized Representative Written, printed, or graphic information appears either on the device itself or on the packaging of each unit or the packaging of multiple devices
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Nomenclature of Medical Devices

Medical device nomenclatures are those products used to prevent, diagnose, treat, and monitor the many diseases known to humankind. Medical devices and medicines play an equally important role in treating huma
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