Two Labs is an industry leader in all facets of pharma services. Our professional, experienced team offers a wealth of skills and knowledge to manage the complexities of pharma product commercialization, market access and market intelligence.
With only a few months left until the final DSCSA compliance deadline, our Director of Serialization, Michael Rowe, shared his thoughts in an Outsourced Pharma article on what companies should be doing now to make sure they’re ready.
Two Labs celebrates a special milestone on July 1st – its 20th anniversary! In the two decades since its founding, the company has enjoyed significant growth in both size and services, and continues to drive innovation in the pursuit of improving the lives of others.
Two Labs is officially unveiling its State Drug Price Transparency (DPT) managed service offerings to help emerging pharmaceutical manufacturers navigate the evolving regulatory landscape imposed by each state’s own independent reporting requirements. Read the press release.
REMS are FDA-mandated, post-marketing safety programs that can be required to appropriately balance a drug’s benefits and risks to support safe use. These safety programs are most often required during the NDA or biologics license application (BLA) process to address risks identified in development.
“We’ve deepened our bench of experts by adding some of the most experienced REMS professionals to our team, including Melissa Landers,” said Howard Miller, CEO of Two Labs.
Emerging manufacturers have a strength in how close to and how passionate they are about the science they are developing. But because they are hyper-focused on the groundbreaking science they’re working on, it can be hard to come up from the weeds to put together the launch support that their product needs. And often, one of the most underestimated parts of that launch plan is medical communications.
Through every step of the commercial journey, Two Labs is your partner in driving success.
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Email: info@twolabs.com
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