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SOLUTIONS & EXPERTISE

Drugs & Biologics

Delivering tailored solutions to our clients to help them navigate regulatory complexity and speed time to marketing authorization
Our expertise

Service Lines

CMC

Chemistry, Manufacturing & Controls (CMC)


Lead technical, quality and regulatory expertise in process development & manufacturing, analytics & formulation development and quality & compliance.

Regulatory_Affairs

Regulatory Affairs Management


Support for the submission lifecycle of drug, biologic, device or combination products from pre-IND through licensure to project timelines, monitoring of project resources, etc.

Nonclinical

Nonclinical Pharmacology/Toxicology


Support for drugs and biologic products; early-stage development planning assistance, nonclinical program review and strategic support for FDA submissions.

Clinical

Clinical Development


Cinical regulatory expertise for products in all stages of clinical development.
Regulatory_Operations

Regulatory Operations


We offer clients an array of tools and services that enhance collaboration, streamline the application drafting process, and reduce regulatory review times.

Our expertise

Biologics Consulting Advantage

Senior Level Talent
Fulltime In-house Consultants
Multidisciplinary Support
Global Portfolio & Proven Track Record 
+100 Years of Combined Experience in Regulatory Projects
Regulatory Support in all Phases of Development
Frequent FDA Interactions
Former FDA Consultants

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