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Biologics and Biosimilar Regulations and Registration in Brazil

According to the Drugs Sector Regulation Chamber (CMED) in 2022, the Brazilian pharmaceutical sector generated US $17.2 billion in sales...

Aug 15, 20233 min read

Nutraceutical Regulations and Registration in Hong Kong (FEHD)

Hong Kong stands out as a dynamic hub in Asia's health supplement market. The trend of consumers embracing a diverse range of dietary...

Aug 9, 20235 min read

Biologics and Biosimilars Regulations, Registration Process in the USA (FDA)

The size of the U.S. biosimilars market, estimated at USD 6.73 billion in 2021, is expected to increase by USD 9.48 billion in 2022 and...

Aug 7, 20233 min read

ANVISA Nutraceutical and Dietary Supplements Regulations in Brazil

In recent years, there has been a growing interest in nutraceuticals and dietary supplements as individuals seek to improve their overall...

Aug 5, 20233 min read

Nutraceutical & Dietary supplements regulations in Mexico

Mexico's nutritional supplements market is set to expand from $9.2 Mn in 2022 to $14.96 Mn by 2030, exhibiting a CAGR of 7.4%. The...

Aug 4, 20235 min read

Pharmaceutical Regulations in Japan

In the Japanese pharmaceutical industry, the journey of developing a new drug is marked by formidable challenges. Statistical data...

Aug 3, 20234 min read

Regulations for Pharmaceutical Registration in Hong Kong

The pharmaceutical market in Hong Kong has reached a significant size, estimated to be around $2.3 billion. This figure highlights the...

Aug 2, 20234 min read

Medicines and Healthcare Products Regulatory Agency (MHRA) Pharmaceutical Regulations and Registration in the UK

In 2024, the Pharmaceuticals market in the United Kingdom is poised for significant growth, with projected revenue expected to reach...

Aug 1, 20237 min read

Pharmaceutical Regulations in European Union

The European pharmaceutical market is expected to reach USD 432.12 billion by 2028, growing at a CAGR of 5.4%. Cancer therapeutics is...

Jul 31, 20235 min read

Medical Device Regulations in Colombia: A Comprehensive Guide

In 2023, the Medical Devices market in Colombia is expected to achieve an impressive revenue milestone of US$2.00 billion. This reflects...

Jul 29, 20237 min read

Pharmaceutical Regulations and Registration in Vietnam

Vietnam is the 7th fastest growing middle-class population in the world and aims to achieve an upper middle class income status by 2035,...

Jul 28, 20235 min read

Pharmaceutical Regulations and Registration in South Korea (MFDS)

The pharmaceutical market in South Korea was estimated to be worth 25.4 trillion South Korean won in 2021. The market size has been...

Jul 25, 20235 min read

Pharmaceutical Regulations and Registration in Malaysia

Malaysia's pharmaceutical market had demonstrated significant growth in recent years, reaching an impressive valuation of $2.9 billion in...

Jul 21, 20237 min read

Medical Devices Regulations and Registration in Indonesia

Medical Devices Regulations and Registration in Indonesia Although the manufacturing sector for medical devices in Indonesia is...

Jul 21, 202310 min read

FAQs - Taiwan (TFDA) Regulations for Medical Device Registration

The regulatory authority responsible for medical device registration in Taiwan is the Taiwan Food and Drug Administration (TFDA).

Jul 20, 202310 min read

FAQ - Singapore (HSA) Regulations for Medical Device Registration

The Health Sciences Authority (HSA) is the regulatory authority responsible for medical device registration in Singapore.

Jul 20, 20238 min read

Medical Device Regulations and Registration Process in Thailand

Medical Device Regulations and Registration Process in Thailand The production of medical devices in Thailand was estimated around 4.9...

Jul 19, 202310 min read

FAQ - Malaysia (MDA) Regulations for Medical Device Registration

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Pharmaceutical Regulations in Thailand

Thailand FDA Regulations for Pharmaceutical Registration

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Medical Device Regulations and Registration Process in Argentina, ANMAT

ANMAT is an Argentine regulatory authority responsible for the regulations governing registration process of medical devices

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