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Independent of the defamation issue, there is
another issue that we need to discuss and that is the allegation by Natco that
Shamnad’s opinions on its lawsuit against Bristol Myers Squibb (BMS) are biased
towards BMS and that he has colluded with them. At some level, I guess this a
professional hazard of running a blog.
This is a very serious allegation and I am
guessing that Shamnad is already taking steps to sue Natco for this potentially
defamatory statement that lacks any factual basis. A close reading of Shamnad’s post (that Natco
took issue with) will reveal that Shamnad also criticizes BMS for their
attempts at drug patent linkage. In pertinent part he states:
“More worrying than Natco's fatal legal
blunder is BMS’ alleged attempt to sneak in drug patent linkage, despite our
courts holding such linkage to have no
valid legal basis in India. Natco alleges that BMS was behind a
show cause issued by the Uttarakhand drug regulator to divest Natco of its
regulatory approval.”
“Given that drug patent linkage has been held
to have no
legal basis in India by both a single judge and an appellate division
bench of the Delhi High Court (and effectively confirmed by the Supreme
Court as well, which refused to admit the appeal from the Division Bench),
BMS will have to answer to a serious charge of bad faith, if Natco's
allegations are indeed true.”
Secondly, some time ago, when BMS had sued
Hetero for this very same patented drug, Shamnad took serious issue with the
attempted drug patent linkage. I repeat from his post here:
“From a policy
perspective too, any such linkage is hugely problematic. Apart from issues of
institutional competence, such linkage contravenes the very essence of the
Bolar provision, a patent defence that permits generic companies to safely
generate regulatory data while the patent is in force and pursue their drug
regulatory application process, so that no time is lost between the expiry of a
patent and the entry of a generic product in the market. Such linkage also
virtually results in the introduction of a "data exclusivity" like
norm, a norm that a government committee (Satwant Reddy Committee) suggested, ought not to be introduced into
India at this stage.”
How then can NATCO claim that Shamnad is
biased towards BMS and against Natco? As an independent academic, he has
expressed his views on a patent litigation of wide public interest. In fact,
this litigation was already in the public eye through mainstream media reports
before SpicyIP covered it, attesting to the fact that it was a matter of public
interest. In fact as I discussed in my earlier post today, mainstream media
reports had pointed to the potentially murky regulatory issues that may arise
as a result of the approval granted in this case. An ET news
report had this to say: “Hyderabad-based generic drugmaker Natco Pharma
has started selling copies of global pharma major Bristol Myers
Squibb's cancer drug
Dasatinib, sold under the brand name of Sprycel,
in the Indian market, after it got a marketing licence from the Uttarakhand
government to sell a generic version of the drug. The move is sure to kick off
a fresh controversy in the regulatory framework over patent issues.”
In the past, drug companies have approached the Drug
Controller General of India (DCGI) to obtain manufacturing licences
for selling drugs in the country. However, this is one of the rarest of rare
case, where a drugmaker has applied for a licence of a patented product through
a state government.” When this report is
viewed in light of the recent Parliamentary Standing Committee document on
regulatory approvals, it is quite clear why there was high public interest in
this case.
Funnily enough, Shamnad was the one who defended
Natco’s right to obtain such approvals legitimately from a State authority and
he is quoted in this news
report as stating:
“A patent expert said that Natco is well within
its right to obtain a licence from a state government to sell the drug in the
Indian markets. The regulator’s only job is to look at safety and efficacy of
drugs, and it is not obliged to look at validity of patents,” said Shamnad
Basheer, professor in Intellectual Property Law, National University of
Judicial Sciences.”
And now, soon
as he criticizes NATCO about one of its cases, he is being accused of bais
against Natco!
Natco also appears to have conveniently
forgotten that Shamnad lavished liberal praise on it for its bold CL strategy
just a few months ago. For instance, in
his interview
to a mainstream media publication, he stated:
“….if the medicine is for the public, what good is it
if the public cannot access it, says intellectual property expert Mr Shamnad
Basheer. The judgment, a baby step for Natco, is, in fact, a giant leap for
rest of the generic pharmaceutical companies, he says.”
In fact, even in the very same post that
Natco has issues with, Shamnad had clearly stated:
“For the longest time, Cipla ranked as our leading
poster child for the debate on patents and access to affordable medicines….
The tables began turning early this
year, when another Indian generic company, Natco filed India's first post TRIPS
compulsory licensing application seeking to slash the patented prices of
Bayers' patented anti-cancer drug, Nexavar. In the wake of the compulsory licensing decision, Natco
catapulted to prominence as our national hero; a bold pharmaceutical
company that refused to cave in to international pressure or to bed foreign
partners, but insisted on pioneering the delivery of cheaper and more
affordable drugs through a new “compulsory licensing” route.”
As we have stated several times on this blog,
as a blog, we are committed to an objective analysis of IP law. If we feel the
need to criticize some company for what we think is poor strategy we will do so
candidly. Being objective does not mean that we cannot express our independent opinion.
As of now Natco may be in serious trouble for
casting aspersions on a reputed academic; particularly since those aspersions
are obviously contradicted by Shamnad’s own earlier writings and views in
favour of Natco.


3 comments:
First of all, any new drug to be introduced in the Indian market needs to approach DCGI for approval and then go for local FDA...what appearing fishy here is how come that local FDA approves a new drug yet to be approved by DCGI..state FDA appears to have violated the basic forms of approval process....
Does bias in opinion invite liability ? I don't think so. He is free to be biased in his opinions if he wants to. Natco can walk away from this blog anytime. If at all Natco wants more limelight, they could sue Google instead. That is exactly what highly media conscious institutes or schools IIPM and GIIS Schools have done, invoking IT Act alongside alleged defamation. They can thank the architects of the IT Act if they find any words "annoying", "insulting" etc. Wonder why "biased" was left out, though.
Does bias in opinion invite liability ? I don't think so. He is free to be biased in his opinions if he wants to. Natco can walk away from this blog anytime. If at all Natco wants more limelight, they could sue Google instead. That is exactly what highly media conscious institutes or schools IIPM and GIIS Schools have done, invoking IT Act alongside alleged defamation. They can thank the architects of the IT Act if they find any words "annoying", "insulting" etc. Wonder why "biased" was left out, though.
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