Pharmaceuticals, Healthcare & Life Sciences
Life-sciences businesses operate across tightly regulated product lifecycles, complex research and commercial arrangements, and increasing convergence between healthcare, technology and data. Clavius advises pharmaceutical, biotechnology, medical-device, healthcare and digital-health businesses, investors and other sector participants on transactions, regulation, commercial arrangements, product risk and disputes.
Our work spans clinical development, licensing and technology transfer, market entry, pricing and reimbursement, product approvals, pharmacovigilance, digital health, data and AI-enabled healthcare, as well as product liability, procurement and contentious matters. We advise across the lifecycle of products and platforms, from development and commercialisation to regulatory scrutiny, enforcement and disputes.
Capabilities
Pharmaceuticals & Biotechnology
Advising pharmaceutical and biotechnology companies on commercial arrangements, licensing, market entry, regulation, product issues and disputes.
Medical Devices & Diagnostics
Advising on regulatory approvals, distribution, commercialisation, product standards, liability and disputes involving medical devices and diagnostic technologies.
Clinical Trials & Research
Advising on clinical-trial arrangements, research collaborations, investigator and site agreements, consent, data use and related regulatory requirements.
Licensing & Technology Transfer
Advising on licensing, technology transfer, research collaboration, know-how, intellectual property and commercialisation arrangements.
Product Approvals & Market Access
Advising on approvals, registrations, regulatory pathways and market-entry issues involving pharmaceutical, healthcare and life-sciences products.
Pricing & Reimbursement
Advising on drug pricing, reimbursement, market-access frameworks and regulatory issues affecting the commercialisation of healthcare products.
CDSCO & Regulatory Compliance
Advising on matters involving the Central Drugs Standard Control Organisation, product regulation, inspections, licensing and related compliance issues.
Pharmacovigilance & Post-Market Obligations
Advising on adverse-event reporting, post-market surveillance, safety obligations, recalls and regulatory response.
Digital Health & HealthTech
Advising on telemedicine, digital therapeutics, health platforms, connected devices and technology-enabled healthcare models.
AI, Data & Healthcare Technology
Advising on AI-enabled diagnostics, health data, privacy, automated tools and the deployment of emerging technologies in healthcare and life sciences.
Healthcare Transactions & Investments
Advising on investments, acquisitions, joint ventures and strategic partnerships involving pharmaceutical, healthcare and life-sciences businesses.
Product Liability & Safety
Advising on product defects, recalls, adverse events, warnings, liability allocation and related disputes.
Public Procurement & Healthcare Tenders
Advising on public procurement, tenders, supply arrangements and disputes involving healthcare products and services.
Healthcare & Life-Sciences Disputes
Representing clients in commercial, regulatory, product, licensing, supply and technology-related disputes across the sector.