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PharmSol, founded in 2004, has grown to become a global pharmaceutical enterprise, offering smart products, and providing bespoke solutions throughout the world. PharmSol’s successful track record is credited to its team’s all-round technical competence, its drive to be the leading choice for clients, its focus on building long term relationships and its longstanding dedication to prosper the pharma industry and community.
Since its inception 20 years ago, PharmSol has treaded a path of perpetual growth, expanding not only its global reach, but also the products and solutions we offer, the diverse yet detailed expertise of our team and the number of clients whose expectations we have exceeded.
Today, PharmSol has earned a worldwide reputation, particularly in the EU market, for developing and registering many first to file products and backward integrating. As a result, we possess a vast portfolio of products and technologies, which are either developed in-house or are co-developments. We endeavor to bring new products to the market and implement new ideas & technologies to meet the needs of the future.
PharmSol is well known for offering integrated solutions with ‘single window’ access to all its clients, ensuring seamless and optimal delivery on all assignments. In key markets and through our experience and operational flexibility, we address challenges of our customers in the areas of pharmaceutical regulations, product development, registration, engineering, market affairs and supply of products.
Year of Establishment: 2004
Total Assets(USD):
Total Number of Staff: 50-100
Main Competitive Advantages: Brand Name,International Approvals/Standards,Experienced R&D Staff,Delivery Term,Contract Manufacturing (CRO,CMO),Reputation,Quality Service
Other Competitive Advantages: PharmSol has earned a reputation of being a one-stop-shop for providing innovative, customized, and cost-effective solutions to the Pharma industry across all geographies. Some of the standard solutions of PharmSol are briefly described below: 1.EU GMP Certification 2.WHO GMP Certification 3.Facility Audits 4.GMP/GDP/GLP Compliance Guidance 5.GDP Audits / CEIV Pharma Audits 6.Technology Transfers 7.Facility Design & Debottlenecking 8.Compliance Guidance during Development of FPs, APIs and KSMs 9.GMP, GxP Training & Development
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Tel: (+86) 400 610 1188
WhatsApp/Telegram/Wechat: +86 13621645194
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