Greenleaf’s comprehensive services and wealth of experience ensure that clients can count on expert guidance as they navigate complex regulatory challenges. Greenleaf professionals work as teams specializing in product quality, manufacturing, and compliance; medical devices and combination products; and drug and biological products.
The firm’s targeted regulatory capabilities include:
- Strategic and technical guidance for medical product development and regulatory review
- Product quality, manufacturing, and compliance
- Compliance assessments, remediation, and inspection readiness
- FDA meeting preparation and communication
- Advisory services
- Medical product labeling and promotion
- Regulatory policy consultation, strategic planning, and communications
- Regulatory benchmarking
To learn more about Greenleaf’s comprehensive services, click here.