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Viswanath Pilla

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Pharma wrap: Divis takes a hit, govt restricts stent makers from pulling out

BUSINESS

Pharma wrap: Divis takes a hit, govt restricts stent makers from pulling out

A round-up of the top stories from the pharma sector.

Glenmark says specialty & innovative products to contribute 30% revenues by 2025

BUSINESS

Glenmark says specialty & innovative products to contribute 30% revenues by 2025

Glemark said it hopes to generate 30 percent of its revenues by 2025 from specialty and innovative products alone. To invest on specialty and innovative pipeline Glenmark said its R&D expenses will stay at roughly 11 – 12 percent of revenues.

DoP invokes emergency powers to block stent makers from withdrawing products

BUSINESS

DoP invokes emergency powers to block stent makers from withdrawing products

The Section 3 of DPCO allows the government in emergency cases to direct any manufacturer to ensure adequate availability of drugs or devices.

NPPA allows Abbott Healthcare to withdraw its popular drug eluting stent

BUSINESS

NPPA allows Abbott Healthcare to withdraw its popular drug eluting stent

Abbott earlier this month approached NPPA seeking to discontinue sale of its Xience Alpine stent from India citing lack sales viability following capping of prices of medical devices by the drug price regulator early this year.

Cadila Healthcare enters pact with Pharm-Aid to produce Chickenpox vaccine in Russia

BUSINESS

Cadila Healthcare enters pact with Pharm-Aid to produce Chickenpox vaccine in Russia

Through this agreement, Zydus gains access to the public and private market segments in the Russian Federation, Belarus, Uzbekistan, Kazakhstan, Armenia and Kyrgyzstan, Cadila Healthcare said in a statement.

Govt to come up with a universal health insurance soon, consultations on with stakeholders

BUSINESS

Govt to come up with a universal health insurance soon, consultations on with stakeholders

Providing universal healthcare has been promise of the Narendra Modi government, but the progress has been patchy.

Biocon's Vizag API plant clears US FDA inspection, shares up

BUSINESS

Biocon's Vizag API plant clears US FDA inspection, shares up

Biocon on Monday said it received zero observations for its active pharmaceutical ingredient (API) plant in Visakhapatnam, Andhra Pradesh.

Pharma weekly wrap: Pharma stocks gain on investor interest due to cheap valuations

BUSINESS

Pharma weekly wrap: Pharma stocks gain on investor interest due to cheap valuations

The BSE Healthcare rose 4.44 percent in the past week, the benchmark Sensex gained 1.49 percent

Timeline of Dr Reddy's regulatory issues and stock price movement

BUSINESS

Timeline of Dr Reddy's regulatory issues and stock price movement

The latest jab is a part of the never-ending saga of regulatory compliance woes the company has been facing starting November 2015

Law to check unethical marketing practices in pharma faces delay due to legal tangle

BUSINESS

Law to check unethical marketing practices in pharma faces delay due to legal tangle

The Law Ministry, which was vetting UCPMP, asked the DoP to rework on the draft code as it wasn’t aligned with the legal framework of Essential Commodities Act.

Biocon gets funding from JDRF to test oral insulin on type-1 diabetes patients

BUSINESS

Biocon gets funding from JDRF to test oral insulin on type-1 diabetes patients

As per the agreement – JDRF or Juvenile Diabetes Research Foundation as it was known will fund Biocon’s global multiple ascending dose study of oral insulin drug candidate to evaluate the safety and tolerability in people with type 1 diabetes.

No change in IPO plans: Aster DM Healthcare set to refile DRHP

BUSINESS

No change in IPO plans: Aster DM Healthcare set to refile DRHP

Aster DM Healthcare filed its draft red herring prospectus (DRHP) for IPO in June 2016 with an intention to raise around Rs 2,000 crore, to provide an exit to existing PE investors, repay debt, and invest on expansion.

Dr Reddy's gets two USFDA observations for Srikakulam plant

BUSINESS

Dr Reddy's gets two USFDA observations for Srikakulam plant

The company said was addressing the observations raised by US FDA without specifying the nature of those observations.

Dishman Pharma gains 20% on US FDA nod to client's cancer drug

BUSINESS

Dishman Pharma gains 20% on US FDA nod to client's cancer drug

"We believe that the increase in the stock price is based upon market estimation that we are one of the suppliers of the API for Zeluja capsules, which got approved by the US FDA," the company said in clarification to stock exchanges. Dishman however did not confirm whether it is the API supplier for Tesaro's Zeluja citing confidentiality agreements.

Sun Pharma seeks marketing approval from European regulator for psoriasis drug

BUSINESS

Sun Pharma seeks marketing approval from European regulator for psoriasis drug

In July 2016, Almirall entered into a licensing agreement with Sun Pharma for the development and commercialisation of tildrakizumab for psoriasis in Europe.

RS passes HIV-AIDS bill to penalise discrimination, make treatment obligatory

HEALTH-TRENDS

RS passes HIV-AIDS bill to penalise discrimination, make treatment obligatory

The bill lays down penal provisions for any discrimination practised against a person with HIV/AIDS and breach of confidentiality.

'Even in US and Europe, we haven't seen such orchestrated action by pharma cos'

BUSINESS

'Even in US and Europe, we haven't seen such orchestrated action by pharma cos'

In an interview to Moneycontrol, David Keeling of McKinsey & Co says Indian pharmaceutical companies have made a lot of progress in terms of quality control, but there is still a long way to go.

New e-platform to help India weed out substandard drugs

BUSINESS

New e-platform to help India weed out substandard drugs

Unlike the US and Europe, India does not currently have a tracking system for the drug supply chain.

Sun Pharma buys Bellus Health arm, gets rights to its experimental kidney drug

BUSINESS

Sun Pharma buys Bellus Health arm, gets rights to its experimental kidney drug

Shigamab is a monoclonal antibody therapy being developed for the treatment of Hemolytic Uremic Syndrome caused by Shiga toxin-producing E. coli (sHUS), a rare disease that principally affects the kidneys and often leads to patients requiring acute dialysis.

Lupin gets US regulator nod for generic oral contraceptive Minastrin 24 Fe

BUSINESS

Lupin gets US regulator nod for generic oral contraceptive Minastrin 24 Fe

Lupin has received approvals for eight products since January this year and has launched seven products including this one.

Why Scott Gottlieb, the new US FDA chief, could be good news for Indian drug makers

BUSINESS

Why Scott Gottlieb, the new US FDA chief, could be good news for Indian drug makers

The US FDA appointment is closely watched by Indian pharmaceutical industry which supplies 40 percent of the generic medications consumed in the US. The generic or copycat drugs account for more than 8 in 10 prescriptions. India has 572 US FDA compliant plants -- the highest outside US.

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