Practice Area
Healthcare, Pharma & Medico-Legal Advisory
The Indian healthcare and pharmaceutical sector operates under a dense regulatory framework. We advise hospitals, pharmaceutical companies, medical device manufacturers, healthcare startups and clinicians.
Our Services
- Pharmaceutical Regulation: Compliance under the Drugs and Cosmetics Act 1940 and the New Drugs & Clinical Trials Rules 2019.
- Medical Device Regulation: Registration, licensing and post-market surveillance under the Medical Devices Rules 2017.
- Clinical Trials Advisory: Regulatory approvals, informed consent, ethics committee compliance.
- Hospital & Clinic Regulation: Clinical Establishments Act, licensing, biomedical waste and NABH.
- Medico-Legal Matters: Consumer complaints, negligence claims and medical council proceedings.
- Health-Data Compliance: DPDP Act application to sensitive personal health data.
Our Approach
Healthcare regulation intersects with patient safety, data protection and complex ethics. We work closely with clinicians and management to design compliance frameworks that hold up in practice.
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