HCT/Ps and Medical Device development
Design Control implementation
Feasibility Testing
Tech Transfer
Mechanisms of action
Disease model systems
Potency assays
Manuscript editing/writing
Histopathology services
Design and Build
Bioprocessing scale-up
Process optimizations
Qualifications & Validations
IP development and support
Patent writing
Preparation of pre-market approval submissions (Medical Device)
TRG requests (HCT/Ps regulated under Section 361)
AATB inspection readiness
U.S. market entry strategies for international start-ups
Creating investor-facing presentations to enable funding mechanisms
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