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New Data Show Foreign Reference Drug Pricing Proposals Would Reduce The Development Of New Innovative Medicines In California By 88%
Mar 24, 2021
Biocom California and the California Life Sciences Association (CLSA) today released data analyzing the potential impact of international reference pricing (foreign price controls) on California’s biopharmaceutical innovation ecosystem, including investment into small company capital formation and the new drug development pipeline.
Read MoreBiotech Takes On Racial And Social Equity. Are The Efforts Sustainable?
Mar 23, 2021
From holding Covid-19 vaccination events in San Francisco’s Tenderloin neighborhood to building programs that target longstanding inequities, the Bay Area biotech industry is stepping into high-profile social issues like never before.
Read MoreCLSA/CLSI Announce Initiation Of Mentoring, Coaching And Professional Development Programs To Help Address Gaps In Representation And Inequity In The California Life Sciences Industry
Mar 18, 2021
The California Life Sciences Association (CLSA)/California Life Sciences Institute (CLSI) announced the creation of the Racial & Social Equity (RSE) Initiative, part of a multi-year program, funded by CLSA/CLSI member companies, with the goal of helping close the gaps in inequity and create a more diverse industry. The RSE Initiative has already surpassed its initial fundraising budget of $1M, with a goal of sustaining 3-year commitments of $1M annually.
Read MoreCLSA Welcomes New Board Members And Kicks Off Robust 2021
Mar 8, 2021
California Life Sciences Association (CLSA), the trade association representing California’s life sciences sector announces the election of three new members to its Board of Directors and the transition of two leadership positions.
Read MoreCLSA Applauds The Release The Medicare Coverage Of Innovative Technology (MCIT) Final Rule
Jan 28, 2021
Earlier this month, the Centers for Medicare and Medicaid Services (CMS) released the final “Medicare Coverage of Innovative Technology (MCIT) and Definition of ‘Reasonable and Necessary” rule (42 CFR Part 405). The rule, if implemented as planned in March of this year, creates a pathway for automatic CMS coverage – for 4 years – of medical devices that receive Food and Drug Administration (FDA) breakthrough technologies program designation and subsequent market authorization through their Expedited Review Approval Process.
Read MoreCalifornia Unveils New Approach To Vaccine Allocation And Distribution
Jan 27, 2021
On Tuesday, January 26, Governor Newsom revised the vaccine rollout plan to help streamline allocation and distribution. Vaccine distribution will now be led by the Government Operations Agency along with CA Health and Human Services and CA Department of Public Health.
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