Laos Alliance Pharmaceutical Group
Pioneering pharmaceutical innovation with cGMP-compliant manufacturing, advanced R&D, and global distribution of high-purity active pharmaceutical ingredients (APIs) and intermediates.
Explore Our ProductsThis page is not the official website. Generated by AI, does not constitute any advice. If needed, please click here to visit the corresponding official website.
Pioneering pharmaceutical innovation with cGMP-compliant manufacturing, advanced R&D, and global distribution of high-purity active pharmaceutical ingredients (APIs) and intermediates.
Explore Our ProductsLaos Alliance Pharmaceutical Group is a leading manufacturer and supplier of high-quality pharmaceutical ingredients and intermediates. With state-of-the-art facilities and a commitment to cGMP standards, we deliver reliable, scalable, and compliant solutions for global pharmaceutical partners.
Our expertise spans research, development, synthesis, and purification of complex molecules, ensuring that every product meets the highest standards of purity, consistency, and safety.
Advanced research in API synthesis
Certified manufacturing standards
High-purity pharmaceutical intermediates and APIs developed for global compliance and therapeutic efficacy.
High-purity PDE5 inhibitor used in erectile dysfunction treatment.
Potent inhibitor of cGMP-specific phosphodiesterase type 5.
Highly selective PDE5 inhibitor with rapid onset.
Selective serotonin reuptake inhibitor (SSRI) for premature ejaculation.
5-alpha-reductase inhibitor used in BPH and hair loss treatment.
Dual inhibitor of 5-alpha-reductase types I and II.
Non-steroidal aromatase inhibitor for hormone receptor-positive breast cancer.
Potent aromatase inhibitor used in oncology applications.
Modern, cGMP-compliant manufacturing and research infrastructure ensuring quality, scalability, and regulatory compliance.
Our GMP-certified production lines ensure batch-to-batch consistency, traceability, and compliance with international regulatory standards including FDA, EMA, and WHO-GMP.
Equipped with modern reactors, purification systems, and analytical instrumentation for efficient development and scale-up of complex synthetic routes.
Manufacturing under strict cGMP guidelines ensures product quality, safety, and regulatory readiness.
Reliable logistics and export experience to North America, Europe, Asia, and beyond.
Dedicated team focused on novel synthesis, process optimization, and impurity profiling.
Products in Portfolio
Countries Served
Years of Expertise
Customer Satisfaction
MOQ varies by product, typically ranging from 10g to 1kg for samples and up to bulk quantities. Contact us for specific details.
Yes, our manufacturing facilities operate under cGMP standards, and we provide full documentation including CoA, MSDS, and TSE/BSE statements.
Yes, we offer custom synthesis and process development for novel or complex molecules. Our R&D team supports route scouting and scale-up.
We employ rigorous QC protocols using HPLC, GC, NMR, and MS to verify identity, purity, and impurity profiles for every batch.
For inquiries, samples, or partnerships, visit our official website to connect with our team.
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