MassBio is gathering input on the FDA’s new PreCheck Program, launched in August 2025 to cut red tape for U.S. biomanufacturers and accelerate U.S. pharmaceutical manufacturing by offering earlier engagement on facility design and CMC readiness. The goal: speed approvals, boost supply chain resilience, and make it easier to build and expand domestic capacity.

Your feedback will directly inform MassBio’s public comments to FDA, ensuring the perspective of Massachusetts’ ecosystem is represented. This survey should take about 10 minutes to complete.

Thank you for sharing your expertise.
Section 1: Background

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* 1. Company Size: How many employees does your company have globally?

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* 2. Years in Business: How long has your company been in operation?

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* 3. Domestic Manufacturing Facilities: Does your company currently operate any U.S.-based manufacturing facilities?

 
14% of survey complete.

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