Mondaq Asia Pacific: Food, Drugs, Healthcare, Life Sciences
Dentons
Recognition of the potential therapeutic benefits of medicinal cannabis for a range of debilitating health conditions has been growing for several years.
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.
Han Kun Law Offices
我国的药品流通市场长期以来处于市场竞争和行政管制并存的状态。政府在引导药品价格形成市场机制的同时,也在积极探索通过行政干预缓#
Han Kun Law Offices
药品技术合同的内容并不仅限于技术的开发或转让,往往还涉及到药品的临床试验申报、注册申请、报产审批、质量体系认证以及经销约定等A
Han Kun Law Offices
与药品技术合同定性问题容易引起争议一样,在药品技术合同纠纷中合同效力问题也经常成为案件的争议焦点。
Han Kun Law Offices
2017年2月13日,国家食品药品监督管理总局对外发布《食品安全欺诈行为查处办法(征求意见稿)》(以下简称"征求意见稿"),对产品欺诈、食品
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.
S.S. Rana & Co. Advocates
Food Safety and Standards Authority of India (hereinafter referred to as "FSSAI") is responsible for regulating genetically modified (hereinafter referred to as "GM") food products.
Singh & Associates
Drug Repurposing, the emerging trend resulting from increasing cost of new drug discovery, researches, trails and generic competition.
Khaitan & Co
The purpose of the Legal Metrology (Packaged Commodities) Rules, 2011 (PCR) is to regulate pre-packaged commodities. Under the PCR, pre-packaged commodities must comply with certain mandatory labelling requirements.
Vaish Associates Advocates
The ‘medical devices' sector has largely enjoyed a free hand from the regulators in India, as the sphere has largely gone unregulated thus far.
Singh & Associates
The Uniform Code of Pharmaceuticals Marketing Practices, 2014 ("UCPMP Code") is a voluntary code issued by the Department Of Pharmaceuticals ("the Department") relating to marketing...
LexOrbis
Rich and varied biodiversity, accompanied by an extensive traditional and contemporary knowledge system makes India one of the most diverse nations in the world in this regard.
Khaitan & Co
Access to affordable and safe medicines is the cornerstone of a vibrant public health framework.
Duane Morris LLP
New Purchased/Referral Care (PRC) regulations give the Indian Health Service (I) , Tribal Organizations (T) and Urban Indian Organizations (U) the ability to cap payment rates...
SKP Business Consulting LLP
Since the government declared medical devices as one of the 25 focus sectors in 2014, the industry has been undergoing significant changes in terms of new policy measures and strengthening of the regulatory framework.
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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.
Singh & Associates
In yet another remarkable development in fostering innovation, creativity and intellectual property protection in India, the Government has announced that an Intellectual Property Exchange...
Lexfield Law Offices
The China Food and Drug Administration on May 12 proposed for the public's comments a draft regulation entitled Relevant Policies for Encouraging Innovations on Drugs and Medical Devices and Protecting Innovators' Rights and Interests ...
Singh & Associates
The Indian pharmaceuticals with its proven product standards and national and International regulatory compliance is the 3rd largest producer and suppliers of cost-effective generic medicines worldwide.
Khaitan & Co
The purpose of the Legal Metrology (Packaged Commodities) Rules, 2011 (PCR) is to regulate pre-packaged commodities. Under the PCR, pre-packaged commodities must comply with certain mandatory labelling requirements.
Corrs Chambers Westgarth
An understanding of the regulatory landscape is necessary before attempting any commercial activities for cannabis.
Singh & Associates
Drug Repurposing, the emerging trend resulting from increasing cost of new drug discovery, researches, trails and generic competition.
Singh & Associates
Research and development especially in the pharmaceutical sector is a time consuming, expensive and a resource intensive process.
S.S. Rana & Co. Advocates
Food Safety and Standards Authority of India (hereinafter referred to as "FSSAI") is responsible for regulating genetically modified (hereinafter referred to as "GM") food products.
Obhan & Associates
The past few years have seen considerable improvement and simplification of the import regulatory framework.
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