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- 1 hr1 hour
- Prices VaryPrices Vary
- Location as required by client
With work in all areas of the drug development process from the IND on through Post-Marketing, LRCG can guide you toward successful development of your product, through a robust Regulatory Strategy. This includes exploring expedited approval pathways, coordinating Health Authority interactions, review of documents, labeling strategy, Regulatory Risk Management, and helping to set-up a Regulatory Department where needed, including creating SOPs and procedures.
Main Office 6005 Main Campus Drive, Lexington, MA, USA
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