Harness the power of catalytic continuous flow reactions to achieve safer, greener, and more efficient chemical manufacturing with enhanced scalability and product quality.
ABOUT SK PHARMTECO
At SK pharmteco our mission is to build strong relationships that create happiness for our customers through the shared goal of producing and delivering life-changing therapies that improve patient outcomes and save lives. With our network of seven global, cutting-edge, facilities our capabilities cover the entire product lifecycle, from initial development to commercial manufacturing. We work with customers in a flexible ‘One Team’ approach, prioritizing collaboration, transparency, and trust to make every interaction easy and seamless.
SK pharmteco offers CDMO services for small molecule, Gene therapy, and Analytical testing, contact our experts to learn more!
FEATURED ARTICLES/BLOGS
-
Overcoming development complexity requires robust process safety. Solutions can safely scale challenging reactions, like click chemistry and cryogenic organometallics, improving efficiency and results.
-
Focusing on solvent management is key to minimizing energy consumption in synthesis. By reducing or replacing solvents, chemists significantly cut both hazardous waste and process energy use.
-
Discover how deep technical knowledge, unmatched capabilities, and a proven safety culture can help protect your process at every stage.
-
The presence of nitrosamine drug substance-related impurities (NDSRIs) in medications has become an urgent issue for the pharmaceutical industry. Understand the acceptable intake (AI) limits.
-
Chemists should strive to design molecules with the least environmental impact. They can utilize toxicologists and data to apply new metrics and issue guidelines to better assess the safety of chemicals.
-
Discover how Simulated Moving Bed (SMB) technology can revolutionize your purification processes by enhancing efficiency, reducing costs, and promoting sustainable practices.
-
Ensure the stability and safety of your drug products by utilizing comprehensive forced degradation and photo-stability testing, guided by ICH and FDA standards, to identify degradation pathways and assess light exposure risks.
-
Chemists and chemical engineers must prioritize sustainable practices by innovating holistic, efficient processes that minimize environmental impact and toxicity, addressing challenges like solvent waste and complex molecule synthesis.
-
Explore our series on key industry advocacy groups to learn how organizations like California Life Sciences (CLS) are driving innovation, fostering growth, and improving patient access in healthcare.
-
Explore the key organizations shaping the pharmaceutical industry, starting with an in-depth look at the European Fine Chemicals Group (EFCG) and the European Chemical Industry Council (Cefic).
-
Discover how to reduce waste, minimize costs, and improve sustainability using the 12 principles of green chemistry. The first principle emphasizes designing chemical processes to eliminate waste creation.
-
Delve into the concept of "Atom Economy," a principle that emphasizes optimizing the incorporation of reactants into the final product to enhance efficiency and minimize waste.
-
Learn from experts and secure reliable testing solutions to eliminate the presence of nitrosamine drug substance-related impurities (NDSRIs) in medications.
CONTACT INFORMATION
SK pharmteco
12460 Akron St #100
Rancho Cordova, CA 95742
Contact: Liza Rivera
WHITEPAPERS
-
Explore how Simulated Moving Bed (SMB) technology can enhance API production while overcoming common misconceptions about chromatographic purification.
POSTERS
-
Control Strategies And Method Development For Nitrosamines In Peptide APIs And Drug Products
Pharmaceutical scientists and engineers must advance robust, sensitive, and efficient nitrosamine detection and control methods to ensure regulatory compliance and safeguard public health in peptide-based drugs.
FEATURED SOLUTIONS
-
In today’s dynamic regulatory environment, keeping pace with compliance requirements and advancements in small molecule analysis is essential.
-
Explore how advanced high-potency capabilities and specialized expertise are driving the development and manufacturing of next-generation ADC payloads and linkers.
-
We specialize in the custom development and manufacturing of small molecule APIs, intermediates, and RSMs, offering scalable solutions from kilograms to multi-ton quantities.
-
SK pharmteco's Texas Facility: A Pillar Of Innovation, Sustainability, And Pharmaceutical Excellence
Discover how SK pharmteco's innovative La Porte, Texas facility combines advanced technology, sustainability, and strategic efficiency to redefine excellence in pharmaceutical manufacturing.
-
Partner with SK pharmteco to harness decades of expertise in safe, scalable, and reliable production of APIs using advanced energetic chemistry, delivering exceptional value from development to commercialization.
-
Partner with SK pharmteco for reliable, ICH-compliant stability testing and storage solutions, supported by expert scientists and fully qualified chambers to ensure the safety and efficacy of your CGMP products.
-
Safely scale the production of APIs using highly energetic chemistry, backed by decades of expertise, controlled processes, and CGMP-compliant conditions from development to commercial manufacturing.
-
Optimize your manufacturing processes and enhance sustainability, while meeting regulatory requirements and minimizing environmental impact.
-
Receive comprehensive stability testing solutions that ensure the safety, efficacy, and quality of your pharmaceutical products at every stage of development by partnering with us.
-
Get access to reliable testing services for the identification and quantification of impurities, ensuring product quality and maintaining patient confidence.
-
Whether your project requires small-scale optimization or large-scale production, SK pharmteco’s expertise ensures precision, reliability, and efficiency at every step of the process.
-
At SK pharmteco, we provide our customers with innovative technology-driven solutions for a reduced time-to-market
-
Continuous flow processing can be integrated into a broader strategy of sustainable manufacturing. By optimizing processes to reduce waste, energy consumption, and environmental impact, pharmaceutical companies can demonstrate their commitment to environmental stewardship and meet regulatory requirements for sustainable practices.