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ESMA seeks more control over energy markets
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Watchdog flags need for more sweeping changes
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Increasing transparency in OTC, physical markets
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By Huw Jones
LONDON, Sept 22 (Reuters) – A temporary brake on gas and electricity derivatives when prices spike could improve how energy markets operate, the European Union’s securities watchdog proposed on Thursday, along with more fundamental changes over time.
The European Securities and Markets Authority (ESMA) said the number of trading halts in energy derivatives has been very low in recent weeks despite rules on circuit breakers already in place and prices racing higher following Russia’s invasion of Ukraine in February.
“It would, therefore, appear useful to consider implementing, on a temporary basis and for energy derivative markets only, a new type of trading halt mechanism,” ESMA said in a statement.
The parameters of such a mechanism should be set at the EU level to apply to all platforms that trade energy derivatives, it said – step that would override exchanges.
“We would envisage these mechanisms to trigger halts for a limited period of time only and in exceptional circumstances, for instance, in case of extreme volatility spikes that may lead to disorderly trading conditions,” ESMA said.
Such a mechanism would need to be implemented as part of emergency measures tackling the current energy crisis, it added.
ESMA was responding to a call for “concrete plans” from the EU’s executive arm, the European Commission, to address issues raised in energy markets by high prices that are forcing governments to offer help to energy companies.
Energy firms sell their output using derivatives markets, requiring them to post “margin” in the form of cash, in practice, to cover positions at clearing houses in case they turn sour.
ESMA said on Thursday it could formally clarify that commercial paper and EU government bonds already qualify as collateral. But it rejected an industry suggestion that EU carbon emission allowances could also be used, given their “high volatility and limited legal protections”.
It also had concerns about making uncollateralised commercial bank guarantees eligible for use as collateral, and said strict conditions would need to apply.
ESMA said such conditions include a time limit on their use, such as for the winter period when stresses in energy markets are expected to continue.
“ESMA believes that prudential requirements should continue to underpin any such exposures and limit banks´ concentration risk, which would then have impact on the practical use of such type of collateral,” the watchdog said, referring to banks’ putting aside capital to cover risks from guarantees turning sour.
Clearing houses should also set limit to ensure that a bank guarantee only represented a “small share” of total initial margin requirements.
Such safeguards will be welcomed by banking regulators in the bloc, clomid tablets worried about a loosening of capital rules.
A top European banking supervisor said lenders should not be encouraged to give guarantees that are not commercially priced and backed by appropriate capital.
EU states hold a summit next week to decide on emergency measures to help energy companies.
MORE TRANSPARENCY
ESMA signalled a need for regulators to have a much broader grip on commodity markets to not just include exchanges, cheap clomid for sale but also over-the-counter or off-exchange trading, and transactions in the physical market.
It was “crucial” that national supervisors in EU states have increased visibility over OTC trades that cover the same market as those traded on exchanges, ESMA said.
Furthermore, physically settled gas and electricity products should at least have to comply with minimum transaction and daily position reporting requirements to increase transparency, it said.
Regulatory waivers to large non-financial firms that can trade in commodity derivatives should be scrapped so they require an investment firm licence, ESMA said.
“This would ensure that such significant entities active in commodity derivatives markets conducting essentially the same business as investment firms would be subject to the stringent requirements established in financial regulation,” ESMA said. (Additional reporting by Francesco Canepa in Frankfurt; Editing by Leslie Adler and Lisa Shumaker)
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By Rocky Swift
TOKYO, Nov 6 (Reuters) – Japan’s Takeda Pharmaceutical Co is looking at making vaccines a core business after completing asset sales to lower debt following its takeover of Shire Plc, Chief Executive Christophe Weber said.
Japan’s biggest drugmaker by revenue recently completed $10 billion in sales of mostly over-the-counter drug assets to reduce debt after its $59 billion purchase of Shire, clomid without dr prescription saying it would focus on five key business areas.
With a dengue fever vaccine in development and deals to make and distribute COVID-19 vaccines in Japan, the company could add a new pillar to its business lineup, Weber said.
“We are in the vaccines business,” Weber told Reuters in an interview. “If the dengue vaccine is successful, yes, it would be a sixth one.”
Takeda’s current five core businesses are oncology, gastroenterology, neuroscience, rare diseases, and where to get clomid plasma-derived therapies.
The company looked into making a COVID-19 vaccine, but determined with its mix of technology and capacity, it was a better fit to work with other developers, Weber said.
Takeda agreed last month to distribute 50 million doses of Moderna Inc’s COVID-19 vaccine in Japan. That was on top of a previous deal to produce Novavax Inc’s COVID-19 candidate, aiming to make 250 million doses.
Takeda’s dengue vaccine candidate, clomid rx TAK-003, is on track for regulatory filing in Asia, Latin America, and the European Union by the end of fiscal 2020, the company said last month. The disease is spread by mosquitoes and order generic clomid is estimated to affect 50 million people a year worldwide with 22,000 deaths.
Following the Shire takeover, Takeda reached its asset disposal goal with the sale of its Japanese consumer healthcare business to Blackstone Group for 242 billion yen ($2.31 billion) announced in August.
The company was not eyeing any more major sell offs, Weber said, saying any such deals would be “very marginal.” (Reporting by Rocky Swift; editing by Jane Wardell)
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Feb 27 (Reuters) – Lucira Health said on Monday the U.S. Food and Drug Administration (FDA) had granted emergency use authorization for its combination diagnostic test for COVID-19 and where can i get generic clomid the flu, where to buy cheap clomid making it the first to be available over-the-counter.
The test – called Lucira COVID-19 & Flu Home Test – is a single-use, at-home rapid test kit that provides results from self-collected nasal swab in about 30 minutes.
Shares of the medical test maker rose more than four-fold to 66 cents in premarket trade.
The FDA’s authorization, which came on Friday, allows the test to be purchased without a prescription and performed completely at home by individuals aged 14 years or older or collected by an adult for children two years or older.
The development comes days after Lucira filed for bankruptcy protection in the United States, where can i get clomid no prescription and said it intended to pursue a sale of its business. “Unfortunately, we were unable to bridge what became a protracted authorization cycle time within our current capital structure and it remained unclear to us when the regulatory authorization would come through,” said CEO Erik Engelson.
The company was hoping to launch the test during autumn last year – in time for the 2022 flu season – but remains confident that the test will play a key role in upcoming periods of severe respiratory disease.
Lucira is also seeking a strategic or financial partner to resume the manufacturing and development of additional home diagnostic tests. (Reporting by Bhanvi Satija and Sriparna Roy in Bengaluru; Editing by Shailesh Kuber and Uttaresh Venkateshwaran)
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