Blog

August 10, 2023
A lot of work goes into getting a new pharma product across the finish line, especially if you’re an emerging manufacturer launching your first product. Every element of a launch strategy is important, but certain components outweigh others.
August 2, 2023
Dive deeper into the nine FDA special designations and programs with Two Labs Drug Pipeline Manager, Ryan Chandanais.
August 1, 2023
The FDA has several special designations or programs to facilitate the development of drugs treating conditions with an unmet medical need. Certain designations can reduce FDA timelines for reviewing a New Drug Application (NDA) or Biologics License Application (BLA).
June 14, 2023
With the industry changing so rapidly – along with patient expectations and prescriber priorities – we felt there was an unmet need to shine a light on programs that are leading the way. Transactional features are now table stakes, and going above and beyond with patient services is how you can help differentiate your product.
May 3, 2023
Tracing is essentially an extension of what companies should already have in place in their suspect drug investigation procedures. The tracing request should not be looked at in a vacuum but as another component of a robust suspect drug investigation.
April 27, 2023
While Tracing hasn’t gotten much airtime outside the tight circle of DSCSA experts – those of us who live and breathe this – the new Tracing requirement is a fundamental process that will become the norm in the pharmaceutical industry.
April 25, 2023
Today’s drug pipeline is in an interesting spot. In 2022, there were only 44 novel new drugs approved, down from 58 in 2020 and 60 in 2021. The decrease is due to several reasons beyond a regulatory COVID lag: a constricted approval pathway, the natural ebb and flow of the industry, and manufacturer funding issues. As the industry grows, it’s becoming harder for companies to go public and raise money like they once could.
April 13, 2023
In 2015, the U.S. government passed the 21st Century Cures Act. In it was a provision called the ‘Open Act,’ designed to increase drug pricing transparency by requiring manufacturers to submit clinical trial results and detailed information on production and R&D costs.
March 21, 2023
Based on Two Labs’ experience supporting 280+ pharmaceutical new product launches, our experts will walk you through the most critical questions to answer when planning a pharma launch strategy.