Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at firstname.lastname@example.org if you need assistance.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
Regulatory News | 07 January 2015 | By Nick Paul Taylor
Welcome to our Asia Regulatory Roundup, our weekly overview of the top regulatory news in Asia.
India has capped compensation for clinical trial volunteers who suffer permanent disability at Rs 66 lakh ($104,000). The figure represents a huge increase over the sums paid out in compensation from 2005 to 2012, but has nonetheless been criticized as being far too low for certain circumstances.
Compensation for permanent disability is now capped at 90% of what can be paid out if a clinical trial participant dies, a stipulation that means all payments will be in the range of $2,800 to $104,000. Trial sponsors must pay compensation regardless of whether they are at fault for the injury, giving India some of the most stringent laws in the world.
However, critics have already questioned the range and how it is calculated. “Going by the official definition, a patient who has lost vision in one eye will be deemed to suffer from 40% disability and entitled to 36% of compensation prescribed in case of death. But if he happens to be a pilot, he will lose his job,” drug regulatory expert CM Gulhati told The Economic Times.
The suitability of the law when it comes to compensation for high earners and for people who require lengthy hospitalizations are two of the main criticisms. Gulhati also questioned why an actuary — the profession that typically determines compensation — was not included on the four-member panel that decided on the methodology.
Even with the caveats, the law still represents a boost for people who have campaigned against what they perceive to be the use of Indians as “guinea pigs” by multinational pharmaceutical companies. Since February 2013, 370 people have died in clinical trials in India. To date, sponsors have paid compensation in 21 cases, DNA India reports.
The Economic TimesI DNA India
The Indian Central Drugs Standard Control Organization (CDSCO) has secured a Rs 900 crore ($142 million) funding boost to strengthen regulatory infrastructure. CDSCO will use the cash to establish a training academy, open new laboratories, modernize existing sites and set up an e-governance mechanism.
Each of the initiatives is intended to address a weakness in the current infrastructure, but anonymous sources within CDSCO and the Indian health ministry have said much more money is needed. “The allocation of Rs 900 crore is the bare minimum that is required for adequate functioning of CDSCO. We had made a proposal to double that sum, which would allow us to train drug inspectors, upgrade and add more laboratories etc,” a senior health ministry official told The Hindu Business Line.
A CDSCO source said the regulator must double the number of inspectors it employs if it is to achieve even a basic level of oversight of manufacturers. State regulators face similar problems. Indian states are set to receive a further $134 million to improve their operations, the weaknesses in which were publicly exposed in the wake of last year’s deaths at a sterilization camp. The All India Drugs Control Officers’ Confederation (AIDCOC) has called on the government to boost regulatory manpower and send state regulators to programs run by their international peers.
The Hindu Business LineI PharmaBiz I More
China’s Food and Drug Administration (CFDA) has told the World Trade Organization (WTO) it plans to revise its requirements for the labeling of cosmetics later this year. CFDA informed WTO’s Committee on Technical Barriers for Trade of its proposal because of the new requirements they place on manufacturers selling cosmetics in China.
The proposals require all labels to be in Chinese, apart from trademarks, foreign company addresses and conventional glossaries, Chemical Watch reports. Manufacturers must also list warnings for certain ingredients found in nail polish, acrylic remover and other flammable products. CFDA will store the new labels in an online system.
CFDA is set to adopt the rules on 1 March 2015 and begin implementing them on 1 July 2015. Companies with products bearing the old label that are already on the market can continue to sell them until 30 June 2016.
Chemical WatchI WTO Document
Pharmaceutical firms in Pakistan have threatened to close their operations after the government pushed ahead with an unpopular pricing policy. The government plans to cap the prices for 318 molecules. Some prices will fall as much as 30%. Further legal action against the government is possible. The Express Tribune
The Indian government has introduced the draft Drug and Cosmetics (Amendment) Bill, 2015 to raise production standards for drugs and medical devices. DNA IndiaI Draft Legislation
China has committed to making it easier for US-based medical device and drug companies to access its markets. The trade agreement aims to speed drug and device approvals. FiercePharmaI More
CFDA has approved Elekta’s Flexitron brachytherapy afterloading platform. Radiation Therapy News
The Drug Controller General of India (DCGI) has asked Chaitanya Hospital to stop providing stem cell treatments. PharmaBiz
CFDA has spotted clusters of adverse events among patients who have been treated with citicoline sodium injection. An investigation found the batch of drugs contained visible foreign matter. CFDA Notice (Chinese)
Manufacturers have blamed price controls for an 80% drop in new drug launches in India in recent years. The Economic Times
A CDSCO investigation has led to 12 people accused of being involved with smuggling drugs from China being held in custody. The New Indian Express
CFDA has adopted a new advertising review seal. CFDA Notice (Chinese)
An Indian parliamentary panel has called for a streamlining of the vaccine clinical trial system. The Economic Times
DCGI has told Johnson & Johnson to share records of the compensation it has paid globally to people who received hip implants. The Indian Express
India’s Apex Committee approved 28 clinical trials. Meeting Minutes I PharmaBiz
Tags: Regulatory Roundup, Asia Regulatory Roundup