active pharmaceutical ingredients (API)
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Historic U.S. Cannabis Rescheduling Unlocks Potential Growth Opportunities for MediPharm Labs, Backed by the Company's Suite of Licenses and Proven U.S. Clinical Trial Supply Experience
Globenewswire· 2025-12-19 13:45
Core Viewpoint - The reclassification of cannabis from Schedule I to Schedule III under the U.S. Controlled Substances Act is a significant milestone that recognizes its medical use and is expected to facilitate clinical research and partnerships for MediPharm Labs [1][4][10]. Industry Impact - The reclassification is anticipated to accelerate cannabis-related medical research by removing barriers that have historically limited U.S. clinical trials, allowing for standardized medical-grade cannabis access [4][5]. - The change may lead to increased interest from institutional investors in research-oriented cannabis companies, as regulatory barriers evolve [10]. Company Positioning - MediPharm Labs is strategically positioned to benefit from this reclassification due to its FDA site registration, Drug Establishment License, and experience in supplying clinical trial materials to the U.S. [2][6]. - The company has a proven track record, having supplied products for over 10 active clinical trials, including significant studies funded by the U.S. National Institutes of Health [7][8]. Research and Development Opportunities - The reclassification is expected to create a pipeline of researchers ready to advance clinical trials and evaluate compliant active pharmaceutical ingredient suppliers [5]. - MediPharm Labs has developed international licensing and regulatory expertise, enabling it to support new research initiatives that require pharmaceutical-grade standards [6][9]. Future Growth Potential - The company anticipates that the reclassification will strengthen its ability to expand U.S. clinical trial partnerships and facilitate significant growth in clinical research [3][10]. - MediPharm Labs' unique combination of experience and regulatory credentials positions it to immediately support new research initiatives in the U.S. and globally [8][9].
China holds all the cards in global pharmaceuticals despite India’s bid to reshuffle the deck
The Economic Times· 2025-11-26 02:28
The urgency of tackling pharmaceutical supplies lies at the heart of the Also Read: Trump delivers another bitter tariff pill. Who’s set to bite the dust?It wasn’t the first time the body has brought up the issue. However, the speed with which the US essentially folded after Beijing expanded export controls on crucial The US and other countries rely heavily on China to make the foundational ingredients for their medicines. Because of its enormous and commoditized industry, which began in the 1950s, China p ...
LLY's $5B Virginia Plant Plan: Will U.S. Manufacturing Shift Pay Off?
ZACKS· 2025-09-17 16:26
Core Insights - Eli Lilly and Company (LLY) plans to invest $5 billion in a new manufacturing facility in Virginia, driven by the Trump administration's push for increased domestic production [1] - The facility is expected to create approximately 650 high-paying manufacturing jobs and 1,800 construction jobs, focusing on active pharmaceutical ingredients (API) and antibody-drug conjugates (ADCs) [2] - This Virginia site is part of Lilly's broader commitment to invest $27 billion in four new manufacturing sites in the U.S. by 2025, contributing to over $50 billion in domestic manufacturing expansion since 2020 [3] Investment and Manufacturing Trends - The U.S. pharmaceutical industry is responding to potential tariffs on imports, with companies like Lilly, J&J, AstraZeneca, GSK, Novartis, and Roche announcing significant investments to boost U.S. manufacturing [5][9] - GSK plans to invest $30 billion in R&D and supply chain infrastructure in the U.S. over the next five years, while AstraZeneca has committed $50 billion by 2030 [6] - J&J announced over $55 billion in investments for U.S. manufacturing and R&D over the next four years, and Roche plans to invest $50 billion, creating over 12,000 jobs [7] Challenges and Market Dynamics - The shift to U.S. production may lead to higher drug prices for consumers due to increased production costs, impacting profit margins for drugmakers [10] - Companies may still rely on international markets for cheaper drugs and key ingredients, necessitating additional incentives like tax breaks and subsidies to encourage domestic production [11] - Lilly's stock has seen a decline of 1.0% this year, compared to a 0.7% decrease in the industry, with its price/earnings ratio at 26.63, significantly higher than the industry average of 14.69 [12][13]
Lilly announces plans to build $5 billion manufacturing facility in Virginia
Prnewswire· 2025-09-16 14:30
Core Points - Eli Lilly and Company plans to build a $5 billion manufacturing facility in Goochland County, Virginia, focusing on active pharmaceutical ingredients (API) for cancer and autoimmune therapies [1][2] - The facility will create 2,450 high-wage jobs, including 650 manufacturing positions and 1,800 construction jobs, contributing significantly to the local economy [4][5] - This site is the first of four new U.S. manufacturing locations Lilly intends to announce this year as part of a broader $50 billion capital expansion commitment since 2020 [2][9] Company Commitment - The investment in Virginia highlights Lilly's commitment to U.S. innovation and manufacturing, aiming to strengthen the domestic supply chain and enhance the delivery of medicines [4][6] - Lilly plans to utilize advanced technologies such as machine learning and AI at the new facility to ensure efficient and safe production processes [6][8] - The company emphasizes sustainability and community engagement, planning to partner with local universities and support educational initiatives [6][8] Economic Impact - For every dollar invested in the Virginia facility, it is expected that up to four dollars will be generated in local economic activity [5] - Each manufacturing job created is projected to support multiple positions in related industries, such as supply chain and logistics [5] - The facility is anticipated to significantly benefit the local economy and strengthen Virginia's position in the pharmaceutical industry [6][8]
MediPharm Announces Voting Results from the 2025 Annual and Special Meeting of Shareholders
Globenewswire· 2025-06-17 14:27
Core Points - MediPharm Labs Corp. held its annual and special meeting where key resolutions were voted on by shareholders [1][2] - A total of 210,726,733 common shares were represented, accounting for 50.76% of the total issued shares [2] - The meeting resulted in the approval of several resolutions including the number of directors, appointment of auditors, election of directors, and unallocated awards under the equity incentive plan [3] Voting Results - The resolution to fix the number of directors at seven was approved with 75.46% voting in favor [5] - All management director nominees were elected with Chris Halyk receiving 144,007,422 votes and Emily Jameson receiving 144,289,930 votes [6] - MNP LLP was appointed as the auditor with 90.78% of votes in favor [7] - The resolution for unallocated awards under the equity incentive plan was narrowly approved with 50.14% voting for and 49.86% against [8] Board Changes - New directors Emily Jameson and John Medland were welcomed to the Board, while Michael Bumby did not stand for re-election [4] Company Overview - MediPharm Labs specializes in the development and manufacture of pharmaceutical-quality cannabis concentrates and advanced derivative products [9] - The company received a Pharmaceutical Drug Establishment License from Health Canada in 2021, making it the only North American company with a commercial-scale GMP license for cannabinoid extraction [10] - In 2023, MediPharm acquired VIVO Cannabis Inc., expanding its reach to medical patients in Canada, Australia, and Germany [11]
MediPharm Labs Cautions Shareholders about Dissident Nominees’ Governance Failures at Check-Cap Ltd.
Globenewswire· 2025-05-23 17:00
Core Viewpoint - MediPharm Labs Corp. is urging shareholders to be cautious regarding the election of three Dissident Nominees associated with Apollo Technology Capital Corporation, citing concerns over their past involvement with Check-Cap Ltd. and its governance issues [1][2][18]. Summary of Recent Events at Check-Cap - Check-Cap has faced significant governance challenges, including poor transparency, high turnover, and questionable cash resource allocation, leading to a decline in shareholder value [3][6]. - A notable incident involved Check-Cap transferring millions of dollars to Apollo and its subsidiaries, which raises concerns about the motives of the Dissident Nominees [4][11]. - The Check-Cap Board approved a $6 million loan to Nobul and transferred $11 million to a segregated account for Nobul's growth initiatives, despite no formal business combination being completed [8][9]. Connections to the Dissident Nominees - Three of the six Dissident Nominees for MediPharm's Board have been directly involved in Check-Cap's governance issues, raising questions about their qualifications to lead another public company [11][14]. - The involvement of these individuals in Check-Cap's tumultuous history suggests a potential risk for MediPharm shareholders [12][18]. Shareholder Voting Assistance - MediPharm encourages shareholders to vote using the GREEN proxy in support of the Company's nominees, emphasizing the importance of disregarding communications from the Dissident Nominees [19][20]. Company Background - MediPharm Labs specializes in the development and manufacture of pharmaceutical-quality cannabis products and has a GMP license from Health Canada, positioning it as a leader in the cannabinoid sector [21][23]. - The Company expanded its reach through the acquisition of VIVO Cannabis Inc., enhancing its presence in the medical cannabis market [24].