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In 2014, Mylan signed an agreement with Gilead to increase access to TAF-based HIV treatments in developing countries.

The SEC opined that there is an unmet need in the country, and the test drug may be an alternative treatment option in patients with uncontrolled severe asthma.

On March 06, 2019, the Central Government proposed labeling specifications for import and manufacturing permission of New Drug Formulation under form 45/46 of Schedule A of Drugs and Cosmetics Act, 1940 ...

The Pharmacovigilance Programme of India, was first introduced in the year 2010 to improve safety of Indian population by monitoring drug related Adverse Drug Reactions collected via ADR monitoring centers ...

Tune into this episode of our podcast series featuring our Partner, Prakriti Jaiswal, as we explore the regulatory and compliance landscape in the Indian healthcare sector. From FDI regulations in pharma...

On Mar 20, 2019, World Health Organization issued guidelines "WHO Consolidated Guidelines on Drug- Resistant Tuberculosis Treatment" to accelerate the treatment of tuberculosis for proper eradication of the multidrug resistant TB ...

In the midst of severe restrictions on physical movement necessitated by the coronavirus (Covid-19) pandemic, e-pharmacies have played an important role in supplying essential medicines to citizens across India.

In the realm of branding, suggestive exert a unique power, entrancing consumers' imaginations while leaving room for interpretations.

The framework was reportedly circulated with companies and government departments in May 2023, but has not been released for public consultation.

We are caught in an escapable network of mutuality, tied in a single garment of destiny.

The Rules introduced the conditions for providing post-trial access of drugs to patients who require it for the first time.

A highly organized sector, the Indian pharmaceutical industry is estimated to be worth $ 4.5 billion, growing at about 8 to 9 percent annually.

The Geographical Indications Of Goods (Registration And Protection) Act, 1999 defines ‘geographical indication' as ‘an indication which identifies such goods as agricultural goods ...

On October 03, 2017, WIPO and the research-based pharmaceutical industry announced launch of a new partnership to promote the accessibility of patent information for health agencies tasked....

Time and again, it has been held by various courts that an unreasonable delay in enforcing a legal right by a person amounts to acquiescence...

The question of granting temporary injunctions is always a knotty one, and requires establishing whether the injunction-seeker has a prima facie case, whether the balance of convenience lies in their favour...

Last year, an interesting issue with respect to copyrightability of unconventional works was raised before EU's highest legal authority, the Court of Justice, European Union

In Zydus Lifesciences Ltd. v. E.R. Squibb and Sons LLC & Ors. (FAO(OS) (COMM) 120/2025, CM APPL. 44383/2025, CM APPL. 44386/2025 & CM APPL. 44388/2025), the Division Bench of the Delhi High Court modified the interim order passed by the Single Judge, who had restrained Zydus from manufacturing, using, offering for sale, selling or importing its biosimilar version of the cancer immunotherapy drug Nivolumab in India.