SupremeCourt

  • Subscribe to our RSS feed.
  • Twitter
  • StumbleUpon
  • Reddit
  • Facebook
  • Digg
Showing posts with label trade. Show all posts
Showing posts with label trade. Show all posts

Thursday, September 5, 2013

Patent Hypocrisy and the Paradox of Indian IP

Posted on 10:40 PM by Unknown
In an earlier email message to the SpicyIP subscribers, I'd linked to an article on Apple vs Samsung and noted as below:

"For those following the Apple vs Samsung patent wars, this latest move by the US government to veto an ITC decision favouring Samsung once again reflects the well known truth that "national" interest trumps all else. 

But then unfortunately, national interest is to be read narrowly as only "US" national interest. For when other countries such as India rely on "national interest" considerations to protect the health and well being of their citizens', they are labelled pirates, outliers and what not.

If there is one consistent take home lesson from the IP and trade wars, it is that of "hypocrisy"!"

I expanded on this sentiment in a recent edit in the Hindu, which I reproduce below.  I begin by noting that the Novartis patent would have been axed in any other jurisdiction had it been as vigorously contested. I then reflect on the paradox of India IP, where there is as much over protection as there is under-protection. Lastly, I take issue with mainstream media coverage of IP issues, where the patent axes are lauded over and the patent wins ignored. For those interested, here is the full text of the Hindu editorial.

Patent Lies and Convenient Truths

Even as the campaign by U.S. drug majors to paint India as a haven for intellectual property pirates intensifies, the government has swung into action to stem the false propaganda. In a potent piece in The Hill’sCongress blog, India’s Ambassador to the U.S. Nirupama Rao argued that India is not on a kamikaze mission to kill all patents. Rather, it has only invalidated those undeserving of protection under India’s stringent statutory standards. And it did so through transparent judicial processes and not through executive fiat as did the U.S. recently, when it overturned a patent ruling from a specialised trade court, the International Trade Commission (ITC), to favour home-grown Apple at the cost of foreign Samsung.

It is difficult to take issue with Ms Rao’s piece, not least because she makes fair and reasonable points; but then again, the qualifier is “reasonable.” In pertinent part, she notes: “The Indian Supreme Court, in a landmark judgment in April, turned down a request by the pharmaceutical company Novartis to retain the patent on a cancer drug because it judged the drug to be an extension of existing medications, not a groundbreaking advancement. In other words, the court reinforced the premium that should rightly be placed on truly valid patents, strengthening, not weakening, their sanctity.”

Problem in perception

I have previously argued that Novartis’ Glivec patent would have got the axe in any other jurisdiction, had it been contested as vigorously. In fact, a U.S. court invalidated a Pfizer patent covering a blood pressure medication (Norvasc) on grounds very similar to the Novartis decision, i.e. mere physical advantages cited for the salt form such as increased stability and solubility were not good enough to merit patent protection.

The problem perhaps is one of perception. Our mainstream media continues to paint a rather harrowing picture of India’s patent ethos, lauding over patent axes and ignoring patent wins. Illustratively, when two of Glaxo’s patents covering a breast cancer drug (Tykerb) were challenged before India’s specialised IP tribunal, IPAB (Intellectual Property Appellate Board), the main patent covering the basic compound was upheld and the secondary patent covering the salt invalidated. While our media hailed the death of the secondary salt patent, they all but ignored the more important primary patent that had been upheld. This creates a rather one-sided perception.

Overprotection

No doubt, India’s IP tribunal has liquidated more patents than its counterparts in other parts of the world, but a dispassionate look at the overall patent numbers will indicate that the situation is not as grim as it is made out to be. Between 2005 and 2011, more than 4,000 patents for pharmaceutical inventions were issued by the Patent Office. Of these, more than 85 per cent were awarded to multinational drug companies. A study done by me in 2009 showed that of all the pharmaceutical patent applications filed, only 0.3 per cent had been challenged. While this percentage may have increased in the last couple of years, I would wager that it has not crossed two per cent!

In fact, if one were to dig deep, one realises that India is as guilty of overprotection as it is of under-protection. I was at a government meeting recently when a representative from a well known copyright collecting society proudly proclaimed that music copyright enforcement had never been better. Courts were issuing extraordinary orders to prevent copyright infringement including orders to block entire websites; orders never known to have been issued anywhere else in the world. What a telling paradox! The so-called developed world looks upon us as an IP deficit nation, little realising that we’re equally guilty of “IP excess.” The sheer number of ex parte restraining orders doled out in patent cases is also testament to this paradox; orders unheard of in any other country and passed without so much as hearing the defendant.

These ex parte orders are severely problematic and one hopes that the Supreme Court puts an end to it. For one, in patent infringement cases, the validity of the patent is almost always challenged. This being so, courts simply cannot afford to issue injunctions without hearing the other side. More egregiously, once issued, it is often difficult and time consuming to reverse such injunctions, and defendants are forced to settle at gunpoint.

As Shashi Tharoor rightly noted in a recent address at IIM Kolkata, everything said about India can be equally true and false. And that is the paradox of this plural nation: there is as much over-protection in intellectual property as there is under-protection!

Speaking of India’s contentious compulsory licensing order in Natco v. Bayer, where after a severely contested quasi-judicial proceeding, the Patent Office issued a licence for a life-saving cancer drug on the grounds of its exorbitant price, Ambassador Rao goes on to note: “Compulsory licensing has been an integral part of the patent regime of many countries for years. Fifteen countries, both developed and developing countries alike, have issued more than 35 compulsory licences.”

Protectionism

What she forgot to mention is that the United States routinely issues such licences, albeit through their courts which refuse to grant patent injunctions on grounds of public interest. In fact, more than a decade ago, the U.S. Secretary of Health threatened to issue a licence against German major Bayer when faced with the Anthrax crisis, forcing it to drop its drug prices. When the U.S. admonishes India on this count asking it to refrain from destroying global innovation imperatives, it strikes one as a classic case of the pot calling the kettle black!

All of which leaves one wondering: why do we continue to reason with a government that has become so adept at playing the Janusian game; resorting to protectionist and public interest measures on its own soil, but lambasting others in the name of free trade and haloed IP rights, when they do so. If there is one consistent theme in the global intellectual property and trade wars, it is that of “hypocrisy”!
Read More
Posted in Novartis, Patent, trade, TRIPS | No comments

Wednesday, June 26, 2013

Part II: Pfizer's testimony leads the way as US pressure on India increases

Posted on 2:34 PM by Unknown
Part I of this looked into some of the claims that Pfizer has made. This part looks into what that testimony has led to.


170 Members of US Congress write to Obama criticizing India's IP regime

The effects of Waldron's testimony, no doubt combined with other lobbying efforts, have led to 170 US Members of Congress writing to President Obama, urging him to ensure 'these issues are raised at the highest levels of the Indian Government and that they are a top priority at the upcoming US-India Strategic dialogue and other bilateral and multilateral meetings.' KEI has made the letter available here.

The letter specifically mentions the Nexavar Compulsory license but without giving reasons other than  it's a "stage three liver and kidney cancer drug". Presumably, the letter is referring to the same reasons that Pfizer's Waldron used in his testimony - ie, the local working requirement. Presumably, they've also skipped over the main reasons for the Nexavar CL (ie, that the medicine was made available to only 2% of the patients and that it was very unreasonably priced at Rs 2.8 lakhs/month).
Regarding the local working requirement - this certainly is controversial. However, there are strong arguments (for eg: 'justified differential treatment' + technology transfer goals of TRIPs) that say it does not fall afoul of Art 27 of TRIPs.
(A similar provision present in Brazilian law was challenged by the US at the WTO, but US withdrew the complaint before any ruling could be given on the matter. Brazil assured US that they would consult with US in case it chose to use that provision to issue a CL).
Though this time they may actually have an argument (as opposed to their claims discussed in part I), once again their confident 'imposition' of this unilateral conclusion on the matter seems disingenuous to me. This opinion is informed by surrounding circumstances as mentioned below.
[On a side note, the Indian Patent Office's latest move of publishing all Statements of Working, is bound to be making a few companies very uncomfortable. Readers can look forward to more from SpicyIP on that front] 

As KEI also points out, "the letter cites the USPTO's statistics claiming that 30 percent of the American work force are employed by intellectual property intensive industries. As noted by KEI previously, however, that USPTO report contained misleading data and more than eighty-three percent of those "IP-intensive" jobs were actually employed by those industries considered to be "trademark intensive"; grocery stores were listed as the top IP-intensive industry."

In any case, this letter is not the only thing that's going around about India's IP regime. A few more IP Reports coming out from US are listed below:

1. Special 301 Report: The latest edition put India on the Priority Watchlist. It too focused on Novartis, Nexaver and data protection. We've covered it before in some detail here,

2. GIPC IP Index: The "Global Intellectual Property Center", run by the US Chamber of Commerce, ranked India last in their inaugural index. They also only ranked 11 countries, of which India was (one of?) the only lower middle income countries. Incidentally, this was also the report that Waldron cited in his testimony before the House of Representatives. The GIPC website issued a statement when India's first Compulsory License was issued (March 2012) saying they were disappointed and that a reliance on compulsory licenses was bad for innovation and didn't go into any other reasons. A 'reliance on CLs' when it was the first ever CL granted that they were talking about? They also issued a statement when the Novartis judgment came out showing their disappointment without giving any reasons other than to state that nearly 40 other countries had given the patent to Novartis. And referring to the Supreme Court as the high court, didn't do anything to boost my confidence in their unsubstantiated opinions either.

3. The IP Commission Report: The Report of the Commission on the Theft of American Intellectual Property : Signed by some current and former governmental higher-ups, this report gives some bizarre recommendations even within US law - like giving IP owners the power to remotely lock up your computer if you try to access their files, and requiring law enforcement to unlock it. With respect to India, it just vaguely mentions how terrible India's IP regime is. Some of their referrals include mention of weak criminal enforcement mechanisms for IP violations, some quotes from USTR's 2013 Special 301 Report, incentivizing provincial and municipal leaders in India to create business environments that protect IP, and a few references to the local working requirement. Techdirt has a bit to say about this report.

4. 2013 National Trade Estimate Report on Foreign Trade Barriers. Issued by the office of US Trade Representative. As per this article, the US government has accused India of lacking “effective protection against unfair commercial use of undisclosed test and other data generated to obtain marketing approval for pharmaceutical and agrochemical products”. It has also stated that India has “weak protection and enforcement of intellectual property rights” and that recent patent-related happenings have only “heightened concerns.”

5. 2013 Joint Strategic Plan on Intellectual Property Enforcement: Prepared by the US IP Enforcement Co-ordinator, this report seemed more well prepared than the first three. Regarding India, it discusses actions taken by the USPTO IP attache in India. While it did voice concerns about IP in India, it seemed a lot more balanced and matter of fact - skipping the alarmist attitude that were present in some of the other reports.


Curiously enough, despite all this, the US-India joint statement issued on the recently concluded US-India Strategic Dialogue makes no mention of patents or pharma or even intellectual property! Meanwhile, Indian Ambassador to US, Nirupama Rao, asserted that the Indian patent regime was not discriminatory against foreign companies and offered to discuss the issue with concerned law makers.

Despite my clear lack of faith in much of these reports and my belief that nearly all of Big Pharma (+ associated lobbyists) efforts are more self serving than anything else, I do believe that India needs to wake up to its healthcare concerns. Given our poverty levels, even if innovation continues to come from the west (despite current drying pipelines), India's not going to be in a position to ensure access to medicines as Big Pharma is hardly likely to deal with developing country diseases and that too at developing country prices. And despite all their claims, patient assistance programs are hardly sufficient even when present. And in any case, charity is hardly a business model for India to rely on.

At the same time, I don't see how promoting stronger patent rights are going to address this concern either. Are programs like OSDD extendable? Private Public Partnerships? Patent pools? Prize systems? Health Impact Fund? Workable theories are out there and solutions need to be worked on. And in the mean time, India needs to ensure it maintains its balance in this innovation versus access debate. 

Read More
Posted in Compulsory Licensing, FTA, Patent, trade, TRIPS | No comments

Part I: Pfizer's testimony leads the way as US pressure on India increases

Posted on 2:32 PM by Unknown
Readers may remember our recent coverage of Pfizer's Chief IP Counsel, Roy Waldron's testimony before a hearing of the US House of Representatives and the heated exchange that followed between Waldron and the Indian Pharmaceutical Alliance (IPA) thereafter. Waldron's main allegations were that the Indian Pharmaceutical patent regime flouted international trade rules and abused the compulsory license system and recommended that the US government use all means at its disposal to get India in line. IPA responded with a strong letter of their own rebutting Pfizer's main points. Since the time of that post, I've also received a copy of Pfizer's response to IPA, dated 23 May 2013 (available here). 

There are a couple of things which stood out to me about Pfizer's statement. Due to the effect that their lobbying is evidently having I will address these in Part I.  Part II will look at the larger context of international pressure that US is trying to create towards establishing a stronger pharma patent regime in India. (Warning: Both posts are fairly long)

Pictured above: Image too humorously relevant to not include
Source


I. Pfizer's response: 
Let me start off by stating that I think India has a long way to go to better the innovation climate for pharmaceutical products. Having said that, aside from Pfizer's growing revenues coinciding with their growing complaints, there are some essential parts of Pfizer's statement where I can't help but think that they are shamelessly engaging in intellectual dishonesty. And this is having dangerous repercussions as will be discussed in part II later. 

Waldron says that India's patent regime has failed to reach standards required by TRIPs due to S.3(d) which allegedly "effectively nullified the contributions of the whole discipline of pharmaceutical sciences". He then points to the Glivec (Novartis) case as an example to prove his point, stating that bioavailability is the holy grail for pharmacists and by any definition is a more therapeutically effective drug. He goes on to state that India's reason and rationale for not complying with the full extent of its TRIPS obligations is 'related to preserving its domestic industry's export markets'. 

Firstly, the Glivec case is a ridiculous example to take, simply because Novartis did not submit data to back up any claim of increased therapeutic efficacy over the former 'known substance' imatinib mesylate. Contrary to what Waldron seems to indicate, the Court had in fact stated that increased bioavailability "can" be linked to therapeutic efficacy. However, as the judgement holds in para 189 “In this case, there is absolutely nothing on this score apart from the adroit submissions of the counsel. No material has been offered to indicate that the beta crystalline form of Imatinib Mesylate will produce an enhanced or superior efficacy (therapeutic) on molecular basis than what could be achieved with Imatinib free base in vivo animal model.” 
To state that a Court should grant a decision in Novartis' favour when they fail to submit evidence to back up a claim is disingenuous. 
Further, Pfizer's claims as to what consists of evergreening should've taken into account their own experience in Pfizer v Apotex, when a US Fed Cir Court ruled that their claimed advantage of increased solubility and stability were not sufficient 'since it found the claimed advantage (better solubility and stability) to be fairly ordinary and the result of mere routine experimentation.' Simply put - trivial changes cannot be passed off as incremental innovation. 

Secondly, for all their declarations of India not fulfilling their WTO TRIPs obligations, Pfizer's submission was clear that they did not want this to go to the WTO dispute settlement body. They do however want US to use 'every available bilateral and multilateral fora to push their message - apparently this doesn't include the WTO forum itself. My opinion is very simply that they know a decision on this issue would likely go in India's favour . This would a) encourage other countries to follow India's role on encouraging only therapeutically innovative pharmaceutical patents, and b) would remove leverage for pushing for (unnecessarily) stronger patent rights. 

Very briefly, the reasons why India's S. 3(d) would likely be held as TRIPs compliant: 

The WTO DSU (Art 3.2) mandates that the existing provisions of the covered agreements are to be clarified in accordance with 'customary rules of interpretation of public international law.' This takes us to the Vienna Convention on the Law of Treaties, 1969 (VCLT), which holds that provisions of a treaty must be interpreted in accordance with the ordinary meaning to be given to the terms of the treaty, “in their context” and “in the light of its object and purpose”. For the object and principles, we turn to Art 7 and 8 of the TRIPS Agreement.
Art 7 (Objectives) emphasizes a balance being struck between technological advancement and social and economic welfare, to the mutual benefit of producers and consumers of technological knowledge.
Art 8 (Principles) also sets forth some of the basic principles of the Agreement, providing that “Members may, in formulating or amending their laws and regulations, adopt measures necessary to protect public health ... provided such measures are consistent with the provisions of this Agreement.”

And of course the Doha Declaration on TRIPs and Public Health unequivocally affirmed that TRIPS "can and should be interpreted and implemented in a manner supportive of WTO members’ right to protect public health and, in particular, to promote access to medicines for all."

Allowing the grant of insufficiently inventive or trivial patents or otherwise lax standards, can result in blocked legitimate competition, discouraging further innovation, market distortions and distort trade and harm for public welfare.  A provision like S.3(d) prevents these harms, and due to its applicability in the pharmaceutical sector, encourages therapeutically beneficial innovation rather than minor changes to known compounds which do not increase health benefits and yet allow monopolistic costs. 
More than mere compliance, I'd go as far as to say that S 3(d) in fact protects the regime that TRIPs sets up.  



As for the question of discrimination in field of technology:
Aside from mandating the three requirements for patentable subject matter (new, inventive step, and capable of industrial application), Art 27.1 mandates that “…patents shall be available for any inventions, whether products or processes, in all fields of technology… ” and “…without discrimination as to … the field of technology…”. It does not however define these requirements, leaving room for interpretation. Art 7 and Art 8 already suggest that Art 27.1 requirements can be crafted to suit member country needs. 
In Canada - Patent Protection of Pharmaceutical Products, the panel described 'discrimination' as "results of the unjustified imposition of differentially disadvantageous treatment." The panel also stated that Art 27 does not prohibit bona fide exceptions to deal with problems that exist only in certain areas. While there is 'differential' treatment, S.3(d) is not 'differentially disadvantaging' in its application. It recognizes that a unique problem exists with chemical entities - i.e., the possibility of 'evergreening' - and puts forward a condition which ensures that these trivial changes cannot be patented. Indian patent law still requires patentable subject matter to be new, involve an inventive step, and be capable of industrial application. On top of this, it is recognizing that ignoring this problem could lead to high public health consequences, and puts forth S.3(d) to handle that situation. Thus is it 'unjustified imposition of differentially disadvantageous treatment'? No. It is simply justified imposition of differential treatment. And it is hopefully something that other countries aren't scared / politically pressured against incorporating in their own patent regimes. The fact that Pfizer/US specifically want to avoid going through the rightful dispute settlement mechanism to decide this, to me, is indication enough that they are well aware of the actual 'strength' of their claims and fear that a panel ruling on this will delegitimize their claims. 


Amongst his other statements, Waldron also claims that India is violating its TRIPs obligations due to its 'local working' requirement for Compulsory licenses, and due to the lack of a provision providing protection for proprietary data. 
There are certainly arguable - to - definitive counters that can be made to most (but not all) of his points. (For eg: See part 3 here, and any of the posts here) I am not going into them for now. I simply wanted to point out that while certain central claims of his statement are plain wrong and others are certainly arguable, this has been portrayed as a real and present 'danger' to the US House of Representatives. This sort of laced rhetoric is not only dangerous for the millions that rely on the low priced drugs that India enables but also because it contributes to the simple minded "Stronger IP = more innovation" rhetoric. It removes focus from the necessity of keeping in mind all the various factors that are required to be considered while formulating pharmaceutical innovation and access to medicine policy. 
Read More
Posted in 3(d), Data Exclusivity, Indian Pharma, IP Policy, Patent, Pharma, trade, TRIPS | No comments

Wednesday, October 10, 2012

Guest Post: Exide v. Exide: Too much Exidement?

Posted on 11:13 PM by Unknown
Our regular guest blogger, Arun Mohan, a practising IP lawyer before the Madras High Court has sent us this very interesting post analysing in detail the recent Exide judgement of the Delhi High Court and its implications for Indian businesses. The case took fifteen years to come to a resolution and even that happened only after one set of lawyers were changed by one of the parties. It helped that the presiding judge was Justice Valmiki Mehta, an exceptional judge known for his 'no-nonsense' attitude in the Delhi High Court. I think this judgment is a very interesting case and highlights some of the challenges of the Indian market. 

Exide v. Exide: Too much Exidement? 

By Arun Mohan

The Delhi High Court has passed another interesting order under the 1958 Act on the issues arising between the domestic and international proprietors of marks. The judgment can be accessed over here.

The facts in the case briefly put are: 

a. An American company (ESBC) was incorporated in the year 1888 and a subsidiary UK company (CESCO) in the year 1891 to manufacture and sell Exide batteries. 

b. In 1947, due to competition issues the cord between the two companies was snapped and the UK company became the individual proprietor of the mark in the UK. 

c. Around such period, CESCO set up factory in India and became proprietor of the mark EXIDE in India. 

d. CESCO also set up 2 group companies in India through which it manufactured and sold batteries. 

e. CESCO and its group companies was taken over by one M/s Chloride Group Limited. 

f. M/s Chloride Group Limited assigned the rights in the mark EXIDE to the plaintiff herein in 1978 and the TM registry records were amended in 1980 to reflect the same. 

The defendant herein is the successor of the American company ESBC, which sought to market EXIDE batteries in India vide a joint collaboration with Tudor Batteries, Spain. The defendant was undisputedly the owner of the EXIDE marks in several countries. The defendant sought to enter the market in or about 1995 citing various governmental barriers as “special circumstances” i.e. it did not abandon the mark as per the Hardie Trading case, to explain its delayed entry and its continued right over the mark EXIDE in India. The plaintiff moved to restrict them from doing the same in 1997. 

The first claim made by the defendant was that of suppression and fraud committed by the plaintiff before the TM Registry. This Order held that such suppression, even if proven would not interfere with the substantive rights of a proprietor and also that Civil Courts do not have jurisdiction to decide on the validity of a mark when a prayer is made for infringement by a registered proprietor. In coming to this conclusion the Court also considered that the defendant had not moved the IPAB till date to challenge the plaintiff’s registration and nor had it sought stay of proceedings under Sec 111. Therefore, the Court held the validity of the plaintiff’s marks to be final. 

In examining whether the defendant company did in fact give a “common law license” to the plaintiff, and if whether the plaintiff’s rights were relatable to the defendant, the Court refreshingly considers relevant commercial scenarios viz., 

a. The defendant did not have any controlling stake over the plaintiff or its predecessors after the split between the UK and US companies. 

b. The defendant never received any consideration from the plaintiff as royalty 

The Court observes that the American company would not have allowed its “most valuable” property to vest with the plaintiff without any control, and therefore there can be no common law license inferred. This observation recognises just how important trademarks are to companies, and that companies if serious about their marks, would be vigilant in maintaining their rights. 

In deciding on special circumstances, the Court observed that there were no direct or indirect bars to import of batteries, and neither was the same demonstrated by the defendant for the purpose of qualifying as ‘special circumstances’. The Court further observed the lacunae in providing financial analysis and statements by the defendant for establishing such special circumstances. 

The Court also held that there was no question of acquiescence by the plaintiff, as the defendant did not sell any goods in India nor did any special circumstances exist. 

The order concludes holding unequivocally in favour of the plaintiff stating that customers and trade would associate EXIDE batteries only with the plaintiff and its predecessors, and it is therefore entitled to injunct the defendants from selling EXIDE batteries in India. 

This judgement is rather simple, stating that the plaintiff being the prior user of the mark in India and the defendant failing to establish any relationship, would be entitled to an order of injunction against the defendants, irrespective of the defendants rights in other countries. Such orders deciding in favour of the Indian proprietor vis-a-vis international proprietors are not unusual and I have worked on a few myself including in this case available over here. 

The fly in the ointment comes in the recent DB order of the Delhi High Court in the Samsung case. The Court therein allowed the sale of imported Samsung products subject to appropriate disclaimers and representations. Could that order be extended to this case? What would be the consequences if I were to import genuine Exide batteries from America, and disclaim that these are imported batteries and have no relation to the Indian company? As per this order, it would appear to be an infringement, whereas the Samsung order offers a glimmer of hope. I do hope this gets appealed to see a further judicial consideration of this issue as such simplistic dichotomy of trademark rights between India and the rest of the world is no longer commercially relevant. The Court also did not consider the trans-border reputation of the defendant, which strangely enough does not appear to have been even argued by the defendant. I would have imagined that this would be the cornerstone of their argument. The case also overlooks the trade’s view of the mark, and most of the conclusions seem to be based on arguments and pleadings. What this case does immediately do is to shake up all holding companies into reviewing their terms with their subsidiaries, distributors and licensees in India.
Read More
Posted in trade, Trademark | No comments
Older Posts Home
Subscribe to: Posts (Atom)

Popular Posts

  • Guest Post: Intermediary liability in defamation cases - Parle, Mouthshut & Visakha cases to clarify the law
    Chaitanya Ramachandran, who has blogged for us previously over here and here , has sent us this excellent guest post analyzing the extent of...
  • SpicyIP Tidbit: An IP Thriller from an IP lawyer
    In an exciting first for the community of intellectual property lawyers in India, Dr. Kalyan Kankanala has penned a thriller novel based, w...
  • Computer Confusion Confounded
    Computer software patentability continues to confound. So says this caustic certiorari petition filed at the US Supreme Court, passed on by ...
  • Full Bench Delhi HC (Design Act)- Reckitt Benkiser India Ltd. v. Wyeth Ltd.
    Image from here A reference (order available here ) was made to a Full Bench of the Delhi High Court to consider as to what amounts to ‘prio...
  • DIPP notifies revocation of Avesthagen patent in Gazette; Patent Office announces new policy for TK related patent applications
    Image from here The Department of Industrial Policy & Promotion (DIPP), Government of India has officially notified, in the Gazette of I...
  • Novelty of Design: Tarun Sethi v. Vikas Budhiraja
    Name of the case : Tarun Sethi & Ors. v. Vikas Budhiraja & Ors. [Delhi High Court CS(OS) 1841/2008] Date of judgment : August 6, 20...
  • Guest Post: Court rejects Apple’s motion for Permanent Injunction against Samsung
    The Apple - Samsung tussle is one that has now almost frequently found its way into our blog . It's being watched so closely due to its ...
  • Rebutting arguments against multiple copyright societies
    Image from here . In response to my l ast post , I received a dismissive comment from Achille Forler, an insider from the music industry, wh...
  • October 2012: Controller's decisions at the IPO
    In the month of October, 2012 the Controller's offices issued 97 decisions.  Out of these 97, 52 decisions were granted (including defer...
  • IP Research Assistant position at IIT, Madras
    Feroz Ali Khader, MHRD IP Chair at the Indian Institute of Technology (IIT) Madras, is looking for research assistants to work on various is...

Categories

  • 126 (1)
  • 3(d) (4)
  • 3(f) (1)
  • 3(i) (1)
  • 3(k) (2)
  • Academic Writing (1)
  • access (10)
  • access to food (1)
  • access to health (3)
  • AIA (1)
  • AIDS/HIV (3)
  • Antitrust (2)
  • Bajaj v LML (1)
  • Basmati Row (2)
  • Biological Diversity (5)
  • Biologics (2)
  • biopiracy (4)
  • biotech (7)
  • Bollywood (25)
  • Broadcasters Rights (5)
  • Budget (1)
  • business method patent (2)
  • Call for papers (2)
  • Cipla (2)
  • Comparative Advertising (4)
  • Competition law (8)
  • Compulsory Licensing (27)
  • condonation of delay (1)
  • Conference (4)
  • Constitution (12)
  • Contracts (1)
  • Controller's decisions (8)
  • Copyright (112)
  • Copyright Amendment Bill 2010 (23)
  • copyright board (4)
  • Copyright Exceptions (6)
  • copyright office (1)
  • Copyright Rules (2013) (5)
  • Copyright Societies (9)
  • Counterfeiting (1)
  • creativity (1)
  • Cross Retaliation (1)
  • csir (4)
  • d (1)
  • D.U. Photocopy Case (16)
  • Darjeeling Tea (3)
  • Data Exclusivity (2)
  • Database (1)
  • DCGI (2)
  • decompilation (2)
  • defamation (9)
  • Designs (3)
  • Designs Act (3)
  • Differential Pricing (2)
  • Dilution (1)
  • Disabilities (3)
  • Disability (2)
  • DMCA (2)
  • Doha Declaration (1)
  • Domain Names (2)
  • Draft Policy of the Indian Government (2)
  • DRM (1)
  • Drug Regulation (7)
  • education (12)
  • Enercon (1)
  • Enforcement (1)
  • EU (2)
  • ex parte (2)
  • exhaustion (3)
  • Exhaustion of Rights (2)
  • Fair Dealing (8)
  • Fair Use (11)
  • Federal Circuit (1)
  • Fees (3)
  • FICCI (7)
  • FRAND (2)
  • free trade agreement (3)
  • FTA (3)
  • G.I. Registry (4)
  • gene sequences (3)
  • Generic medicine (4)
  • Geographical Indication (14)
  • Gilead (1)
  • Glenmark (5)
  • Gopika (34)
  • Guest post (11)
  • guidelines (1)
  • GWU-CII (1)
  • Herceptin (1)
  • hot news (3)
  • ICANN (1)
  • incremental innovation (1)
  • independence (1)
  • india (5)
  • Indian Government (1)
  • Indian patent litigation (27)
  • Indian Pharma (35)
  • Injunction (10)
  • Innovation (7)
  • INTA (1)
  • Intermediaries (10)
  • internet (11)
  • Internet Access Providers (IAPs) (5)
  • Internet Censorship (7)
  • IP scholarship (3)
  • IP aware (4)
  • IP Course (3)
  • IP Education (1)
  • IP Policy (11)
  • IP update (4)
  • ip writing competition (1)
  • IPAB (34)
  • ipchair (1)
  • IPO (1)
  • IPRS (5)
  • IT Act (1)
  • Journal (2)
  • judicial independence (3)
  • Jurisdiction (1)
  • Kruttika (4)
  • Legal Education (3)
  • Legal Research Tools (1)
  • Legal Scholarship (2)
  • library (2)
  • Licensing (7)
  • Madhulika (20)
  • mathematical methods (1)
  • Media law (3)
  • medical method (1)
  • Merck (4)
  • mhrd ip chair (1)
  • Microsoft (3)
  • Middle Path (1)
  • Moral Rights (2)
  • Movies (18)
  • musical work (2)
  • nanotechnology (1)
  • Natco (3)
  • natco defamation suit (5)
  • natco vs bayer (4)
  • need for transparency (1)
  • Novartis (8)
  • Novartis patent case in India (11)
  • NPEs (2)
  • nujs (1)
  • NUJS Conference (2)
  • Obituary (1)
  • obviousness (7)
  • Off-Topic (2)
  • online course (4)
  • Open Access (6)
  • Open Source (2)
  • Opposition (3)
  • Parallel Imports (4)
  • Parliament (1)
  • passing off (5)
  • Patent (52)
  • Patent act (10)
  • patent agent (5)
  • patent agent exam (9)
  • patent agent exam qualifications (3)
  • patent infringement (5)
  • Patent Licensing (2)
  • Patent litigation (2)
  • Patent Office (19)
  • patent pool (3)
  • Patent Prosecution (7)
  • Patent rules (2)
  • Patent Strategies (8)
  • Patents (9)
  • pegasus (1)
  • Personality Rights (1)
  • Pfizer (1)
  • Pharma (18)
  • Piracy (5)
  • plagiarism (3)
  • Plant Variety Protection (2)
  • post grant (1)
  • Prashant (2)
  • Preventive Detention (1)
  • Price Control (6)
  • prior publication (1)
  • Privacy (3)
  • Prizes (1)
  • public health (3)
  • Public Interest (4)
  • Publicity Rights (4)
  • Publishing (3)
  • radio (2)
  • Rajiv (18)
  • Rectification Petition (2)
  • Rejection (1)
  • research (3)
  • reverse engineering (2)
  • revocation (4)
  • rip (1)
  • Roche (2)
  • Roche vs Cipla (1)
  • Royalty (2)
  • RTI (2)
  • Scholarship (4)
  • section 16 (1)
  • Section 3(d) (7)
  • section 8 (6)
  • shamnad (11)
  • Shan Kohli (4)
  • Shouvik Kumar Guha (30)
  • Smartphones/Tablets (2)
  • Social Innovation (1)
  • Software (10)
  • software enforcement (3)
  • software patent (3)
  • Special 301 Report (1)
  • Spicy Tidbits (6)
  • spicyip (1)
  • SpicyIP Accolades (1)
  • SpicyIP Announcements (9)
  • SpicyIP Case (1)
  • SpicyIP Cases (3)
  • spicyip commiseration (1)
  • SpicyIP Events (11)
  • SpicyIP Fellowship (5)
  • SpicyIP Guest Series (22)
  • SpicyIP Interview (2)
  • SpicyIP Jobs (4)
  • SpicyIP Jobs/General (2)
  • SpicyIP Review (1)
  • SpicyIP Tidbits (11)
  • SpicyIP Weekly Review (27)
  • Statutory Licensing (1)
  • STI Policy 2013 (4)
  • Sugen (3)
  • Supreme Court of India (5)
  • Swaraj (19)
  • Tarnishment (1)
  • Technology (6)
  • Technology Transfer (5)
  • TKDL (5)
  • TPP (1)
  • trade (4)
  • Trade Secret Protection (1)
  • Trademark (59)
  • Trademark dilution (1)
  • Trademark Registry (9)
  • Traditional Knowledge (7)
  • Transparency (5)
  • treaty (1)
  • trial (1)
  • tribunals (2)
  • TRIPS (11)
  • UK (3)
  • unfair competition (5)
  • UNFCCC (1)
  • Universities Research and Innovation Bill (2)
  • US (1)
  • US Patent Reform (1)
  • US Supreme Court (3)
  • viva (3)
  • WIPO (5)
  • Working a Patent (2)
  • Workshop (4)
  • writ (1)
  • WTO (1)

Blog Archive

  • ▼  2013 (364)
    • ▼  September (13)
      • Guest Post: Intermediary liability in defamation c...
      • Breaking News: Kerala HC ends suo moto proceedings...
      • Copyright Amendments: A Fair Balance?
      • Eucador Trademark Registry decision on Gandhi Trad...
      • Computer Confusion Confounded
      • Microsoft - Nokia deal: A paradigm shift in the st...
      • IP Research Assistant position at IIT, Madras
      • Patent Hypocrisy and the Paradox of Indian IP
      • SpicyIP Tidbit: Zanjeer- Salim/Javed Settle with P...
      • Delhi HC rejects the "Hot News" Doctrine: A Summary
      • Bombay HC: Remake Zanjeer to be released
      • IPAB revocation of Allergan’s Combigan patent: Vie...
      • Cold News for Cricket Score Monopolies: India Reje...
    • ►  August (41)
    • ►  July (36)
    • ►  June (36)
    • ►  May (32)
    • ►  April (51)
    • ►  March (66)
    • ►  February (40)
    • ►  January (49)
  • ►  2012 (131)
    • ►  December (29)
    • ►  November (42)
    • ►  October (50)
    • ►  September (10)
Powered by Blogger.