As a critical component of the healthcare industry, participants in the Life Sciences sector devote most of their efforts into the various stages of research, development, technology transfer and commercialization of products and services designed to treat, prevent and cure disease, rehabilitate healthy function, and sustain life. Life Sciences activities are governed by a myriad of international and domestic laws and regulations – many of which are currently evolving to keep up with advancing technology. From an ethical as well as from a legal perspective, operating within these laws is of paramount importance. Hancock Daniel’s Life Sciences attorneys offer pragmatic advice and a depth of perspective gained only through significant experience in the field. Where needed, they assist with effective regulatory engagement to gain clarity and advance business objectives.
Life Sciences Areas:
- Regulatory Compliance
- Clinical Research
- FDA- Regulated Product Development
- Marketing and Distribution
- Pharmacy Operations
- Regulatory Engagements
- 503A and 503B Compounding Pharmacies
- Federal and State Auditing and Compliance Programs
- Telehealth
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