Mondaq Asia Pacific: Food, Drugs, Healthcare, Life Sciences
Clayton Utz
The TGA is proposing a standardised process for pre-market assessments with legislated timeframes and fee structures.
Clayton Utz
These proposed changes to the Therapeutic Goods Advertising Code are intended to promote four clear objectives.
Carroll & O'Dea
Despite the popularity of cosmetic procedures, the industry in Australia is less regulated than other areas of medicine.
Holman Webb
There are significant legal issues to consider for marketers of therapeutic goods.
Ropes & Gray LLP
In addition, the Final Policy attempts to strike a balance between the potentially conflicting interest of innovative and generic drug manufacturers.
McDermott Will & Emery
Hospitals in China differ greatly from those in the west with respect to their relationships with physicians and patients; but they also share some of the same legal challenges faced by western hospitals.
Ropes & Gray LLP
In China, medical devices are divided into three regulatory classes based on the identified risks associated with the devices.
Ropes & Gray LLP
On May 19, 2017, China's State Council promulgated the amendments to the 2014 Regulation on the Supervision and Administration of Medical Devices ("the Amendments"), which became effective immediately.
Ropes & Gray LLP
Further legislative initiatives will be arranged if any parts of the draft policies contradict the current CFDA regulations.
Singh & Associates
An ePharmacy is an online pharmacy, Internet pharmacy or mail-order pharmacy that operates over the Internet and sends the orders to customers through the mail or shipping companies.
Rajeshwari & Associates
Internet has silently crept into our lives to an extent that not just household items, but drugs and other wellness products can be purchased online easily.
Khaitan & Co
The healthcare industry in India has seen an impressive growth trajectory in the past few years and the Indian medical devices market has been the sunrise segment in the healthcare space.
Clyde & Co
India is at the cusp of establishing a robust and organized food sector. Many global players such as Amazon (USA), Nestle (Switzerland), Unilever (United Kingdom) and Yakult (Japan) are playing a key role...
Clyde & Co
This edition brings to our readers a featured article titled "Foreign Investment in the Food Sector – the Present and the Road Ahead".
PSA
E-pharmacies or online pharmacies have been a subject matter of debate in India for the last 3-4 years. Their offline counterparts have been lobbying to get a blanket ban on any online sale of drugs, whether prescription or over-the-counter.
Nishith Desai Associates
After the recent move to fix the price of the coronary stents, the Indian government has imposed a price ceiling on knee replacement systems for a period of one year by way of a notification dated August 17, 2017.
Remfry & Sagar
Trastuzumab - a breast cancer drug manufactured by Roche and Genentech Inc., is imported and marketed in India by Roche Products (India) Private Limited under the brand names Herceptin, Herclon and Biceltis.
Nishith Desai Associates
On June 23 2017, the Government of India notified an amendment to a law that regulates contents of labels of all pre-packaged goods sold in India.
S.S. Rana & Co. Advocates
On May 21, 2003, the World Health Organization Framework Convention on Tobacco Control (hereinafter referred to as the ‘FCTC Treaty') was adopted by the 56th World Health Assembly.
Kochhar & Co.
The Legal Metrology (Packaged Commodities) Rules, 2011 ("Packaging Rules") regulate pre-packaged commodities in India and inter – alia mandate certain labeling requirements prior to sale of such commodities.
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Holman Webb
A genomic profile may help a doctor make personalised health decisions, but also raises a number of ethical challenges.
Shelston IP
The TPPA-11 is what remains of the Trans-Pacific Partnership (TPP) Free Trade Agreement following the US withdrawal.
Corrs Chambers Westgarth
This article is an overview of key proposed IP changes, the likely impact and five takeaways for your organisation.
Holman Webb
Future action for non-compliance with the ACL in the marketing of therapeutic goods may result in much higher penalties.
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The article considers the responses to some of the key recommendations and potential implications of these responses.
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The Appeal decision confirms the need to understand medical malpractice and civil liability policy terms and conditions.
Shelston IP
The outcome of consultation with the sector will not be known for some time and progress will be monitored with interest.
Holman Webb
This case provides clear guidance of the type of complaint which can easily be characterised as not made in good faith.
Holman Webb
When the treatment rendered is consistent, consent will not be vitiated if a different surgeon performs the procedure.
Holman Webb
There are significant legal issues to consider for marketers of therapeutic goods.
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