Process

Developability and manufacturability considerations

Development, qualification, and validation of analytical methods

Analytical

Formulation

Drug Substance and Drug Product Manufacturing

Molecule stabilization considerations

Supporting clinical as well as commercial requirements

Quality

Due diligence support

Regulatory

Global markets

Shipping Logistics

Getting your biologic to the right location on time

Continuous Improvement

Implementing process improvements, Six Sigma, Lean, and Agile systems

Negotiation

Contracts and agreements

Supporting growth through Licensing, M&As, and Divestiture

Prospecting and qualifying; converting qualified leads into your customers

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Management

Supply Chain - External Manufacturing - Supplier Relationship